US20040259101A1 - Methods for disease screening - Google Patents

Methods for disease screening Download PDF

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US20040259101A1
US20040259101A1 US10/601,132 US60113203A US2004259101A1 US 20040259101 A1 US20040259101 A1 US 20040259101A1 US 60113203 A US60113203 A US 60113203A US 2004259101 A1 US2004259101 A1 US 2004259101A1
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patient
sample
amount
nucleic acid
disease
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Anthony Shuber
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Exact Sciences Corp
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Shuber Anthony P.
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Priority to US10/601,132 priority Critical patent/US20040259101A1/en
Priority to EP04776825A priority patent/EP1644529A2/en
Priority to AU2004250246A priority patent/AU2004250246A1/en
Priority to PCT/US2004/019732 priority patent/WO2004113574A2/en
Publication of US20040259101A1 publication Critical patent/US20040259101A1/en
Assigned to EXACT SCIENCES CORPORATION reassignment EXACT SCIENCES CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SHUBER, ANTHONY P.
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/156Polymorphic or mutational markers

Definitions

  • This invention generally relates to methods for screening for disease in a patient. More specifically, this invention relates to the quantitative analysis of nucleic acids in a patient sample, and optionally, performing additional disease testing.
  • Current disease screening methods include, for example, invasive tests and cellular-based assays.
  • invasive tests include physical examination and biopsy of potentially-cancerous tissue.
  • cellular-based assays include analysis of DNA, RNA, chromosomes, proteins, and certain metabolites to detect heritable disease-related genotypes, mutations, phenotypes, or karyotypes for clinical purposes.
  • Genetic assays for cancer often involve probing specific genes for previously identified mutations. For example, a number of genetic mutations, including alterations in the BAT-26 segment of the MSH2 mismatch repair gene, the p53 gene, the ras oncogene, and the APC tumor suppressor gene have been associated with the multi-step pathway leading to cancer.
  • Known screening methods contain a number of practical limitations. For example, invasive cancer screening procedures are often expensive and can result in significant patient discomfort or possibly severe medical complications. Further, the cost of commercially available genetic assays for disease screening can range from hundreds to thousands of dollars, depending on the sizes of the genes and the numbers of mutations tested. Accordingly, there is a need in the art for relatively simple and inexpensive screening methods that can be administered to a patient prior to performing additional disease testing. Such methods are provided herein.
  • methods of the invention comprise quantifying an amount of nucleic acid in a patient sample. If the amount of nucleic acid in the sample is greater than a predetermined threshold amount, then the patient is identified as a candidate for additional disease testing.
  • the predetermined threshold amount is preferably set so that patient samples having an amount of nucleic acid lower than the predetermined threshold amount can be identified as being relatively disease-free.
  • Methods of the invention are useful as screening techniques for any disease, including cancer, such as, but not limited to, colorectal cancer.
  • Methods of the invention can be used to identify a subset of a patients in a population that are relatively disease-free. In certain embodiments, this patient subset does not undergo additional disease testing, although additional disease testing may be performed if desired. In one embodiment, the predetermined threshold amount is set so that approximately 10-20% of patients in a population can be identified as being relatively disease-free using methods of the invention. Therefore, the present invention provides cost-effective screening methods to determine if a patient is a candidate for additional disease testing.
  • Methods of the invention provide that the quantitative amount of nucleic acid in a sample is indicative of disease status of the patient from whom the sample was obtained.
  • tissue or body fluid samples especially those described below, contain shed cellular debris.
  • samples containing cellular debris from such patients have an increased amount of nucleic acid relative to samples from certain healthy patients.
  • Methods of the invention are practiced by quantifying an amount of nucleic acid in a sample and comparing the measured amount to a predetermined threshold amount.
  • a positive screen represents a measured amount of nucleic acid greater than the predetermined threshold amount.
  • a negative screen represents a measured amount of nucleic acid lower than the predetermined threshold amount.
  • the predetermined threshold amount can be determined by empirical means. For example, the predetermined threshold amount can be determined by amplifying a particular genetic locus in a sample from each of a population of normal and diseased patients and quantitatively analyzing the amount of DNA in each of the patients in the population. The predetermined threshold amount is preferably set below the measured amount of nucleic acid in any of the diseased patient samples. Once the predetermined threshold amount has been determined, it can be used as the basis for further screening.
  • the amount of nucleic acid in a patient sample is quantitatively measured.
  • the amount of nucleic acid in a patient sample is quantitatively measured by calculating a number of genome equivalents (as used herein, genome equivalents is abbreviated “GE”) in a sample.
  • GE genome equivalents
  • one GE is equivalent to the amount of genomic DNA present in one normal cell.
  • a measurement of 100 GEs in a sample indicates that the sample contains approximately the same amount of DNA as would be found in 100 cells.
  • the number of GEs can be related to the number of copies of a particular segment of the genome, such as a particular gene, exon, or intron.
  • the number of GEs can be calculated by amplifying one or more genetic loci thought to be present in a sample and quantitatively analyzing the amount of genomic DNA in the sample through any quantitative process known in the art. In certain embodiments of the invention, one GE is the equivalent of about 7 picograms of DNA. In some embodiments, an amplification reaction is conducted at a single genomic locus to amplify a fragment of a specific length. Typically, fragments of 200 bp or less at the same genomic locus are amplified. There is generally a one-to-one correspondence between the amplification of a single 200 bp fragment and one genome equivalent.
  • GE scores will vary depending on a number of factors, including, but not limited to, preparation methods, amplification methods, and quantitative analysis methods.
  • the quantity of human genomic DNA (or other patient DNA, such as animal DNA) in a heterogeneous sample comprising shed cells or cellular debris is measured.
  • Additional disease testing of the invention includes, but is not limited to, genetic assays, diagnostic evaluation, and physical examination.
  • Methods of the invention are useful as general disease screening techniques, and are useful as screens for a wide-range of disease states.
  • Methods of the inventions are also useful as screening techniques for the presence of cancer and pre-cancer, and are especially useful as screening techniques for colorectal cancer and pre-cancer.
  • the invention provides methods for screening a patient for the presence of disease including the steps of measuring a quantitative amount of nucleic acid in a patient sample comprising shed cells or cellular debris, and identifying the patient as a candidate for additional disease testing if the amount of nucleic acid is above a predetermined threshold amount.
  • the nucleic acid can be genomic DNA.
  • the measuring step can include determining a number of genome equivalents.
  • the method can further include the step of performing an assay on a sample from the patient if the patient is identified as a candidate for additional disease testing.
  • This assay can be a DNA integrity assay, mutation detection assay, enumerated loss of heterozygosity (LOH) assay, expression assay, and/or fluorescent in-situ hybridization (FISH) assay.
  • LHO loss of heterozygosity
  • FISH fluorescent in-situ hybridization
  • the assay can detect mutations at any genetic locus such as, but not limited to, p53, ras, APC, DCC, and/or BAT-26.
  • the method can further include the step of performing a diagnostic examination on the patient if the patient is identified as a candidate for additional disease testing.
  • the step of performing a diagnostic examination can be a colonoscopy, a sigmoidoscopy, a fecal occult blood testing and/or an upper gastrointestinal evaluation.
  • the patient sample can be stool, sputum, pancreatic fluid, bile, lymph, blood (such as blood serum or blood plasma), urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and/or pus.
  • the disease can be cancer or pre-cancer.
  • the cancer can be colorectal cancer, lung cancer, esophageal cancer, prostrate cancer, stomach cancer, pancreatic cancer, liver cancer, and/or lymphoma.
  • the invention provides methods for screening a patient for the presence of abnormal proliferating cells including the steps of measuring a quantitative amount of nucleic acid in a patient sample including shed cells or cellular debris, and identifying a positive screen as a sample in which the amount of nucleic acid is above a predetermined threshold amount.
  • the nucleic acid can be genomic DNA.
  • the measuring can be determining a number of genomic equivalents.
  • the method can further include the step of performing an assay on a sample from the patient if a positive screen is identified in the identifying step.
  • This assay can be a DNA integrity assay, mutation detection, enumerated LOH, expression assays, and FISH.
  • This assay also can be one that detects mutations at a genetic locus including p53, ras, APC, DCC, and/or BAT-26.
  • the method can further include the step of performing a diagnostic examination on the patient if a positive screen is identified in the identifying step.
  • the step of performing a diagnostic examination can be a colonoscopy, a sigmoidoscopy, a fecal occult blood testing and/or an upper gastrointestinal evaluation.
  • the patient sample can be stool, sputum, pancreatic fluid, bile, lymph, blood (such as blood serum or blood plasma), urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and/or pus.
  • the invention provides methods for diagnosing the state of health of a patient including the steps of measuring a quantitative amount of nucleic acid in a patient sample including shed cells or cellular debris, and performing an assay on a sample from the patient if the amount of nucleic acid is above a predetermined threshold amount such that the state of health of a patient is determined.
  • the nucleic acid can be genomic DNA.
  • the measuring can include determining a number of genome equivalents.
  • the assay can be a DNA integrity assay, mutation detection, enumerated LOH, expression assays, and/or FISH.
  • the assay can detect mutations at a genetic locus including p53, ras, APC, DCC, and/or BAT-26.
  • the method can further include performing a diagnostic examination on the patient.
  • the diagnostic examination can be a colonoscopy, a sigmoidoscopy, a fecal occult blood testing, and/or an upper gastrointestinal evaluation.
  • the patient sample can be stool, sputum, pancreatic fluid, bile, lymph, blood (such as blood serum or blood plasma), urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and/or pus.
  • blood such as blood serum or blood plasma
  • urine cerebrospinal fluid
  • seminal fluid saliva
  • breast nipple aspirate and/or pus.
  • FIG. 1 is a flowchart representation of method steps for diagnosing disease in a patient in accordance with one embodiment of the invention.
  • FIG. 2 is a flowchart representation of method steps for diagnosing disease in a patient in accordance with another embodiment of the invention.
  • FIG. 3 is a flowchart representation of method steps for diagnosing disease in a patient in accordance with a further embodiment of the invention.
  • FIG. 4 is a flowchart representation of method steps for diagnosing disease in a patient in accordance with another embodiment of the invention.
  • FIG. 5 is a flowchart representation of method steps for diagnosing colorectal cancer in accordance with one particular embodiment of the invention.
  • Methods of the present invention are useful in screening for disease in a patient.
  • Methods of the invention provide that the amount of nucleic acid in a sample comprising shed cellular material is indicative of the disease status of the patient from whom the sample was obtained.
  • methods of the invention comprise measuring the quantitative amount of nucleic acid in a sample from a patient. If the measured amount of nucleic acid in the sample is greater than a predetermined threshold amount, then additional disease testing is performed on the patient. The additional disease testing includes, for example, genetic assays and physical examination. If the measured amount of nucleic acid in the sample is lower than a predetermined threshold amount, then no additional disease testing is necessary, although it can be conducted if desired. Accordingly, the present invention provides relatively cost-effective screening methods that can be administered to a patient prior to performing additional disease testing on the patient.
  • methods of the invention comprise screening a patient sample by conducting an amplification reaction using as a template a nucleic acid suspected or expected to be in the sample; measuring a quantitative amount of amplification product obtained; comparing the amount of amplification product obtained to a predetermined threshold amount; and identifying the patient as a candidate for additional disease testing if the amount of amplification product is greater than the predetermined threshold amount.
  • a predetermined threshold amount is determined by empirical means. Also in certain embodiments, a predetermined threshold amount is determined by reference to the art.
  • One method of the invention includes conducting in a tissue or body fluid sample an amplification reaction using as a template a nucleic acid locus suspected to be in the sample. If the amount of amplification product (amplicon) is greater than a predetermined threshold amount, then additional testing may be performed on a patient.
  • the amplification reaction can be a polymerase chain reaction (PCR). Methods for conducting PCR are provided in U.S. Pat. No. 4,683,202, incorporated by reference herein.
  • the amplification reaction can be reverse transcriptase PCR. Primers are designed to amplify the locus or loci chosen for analysis.
  • genomic locus is any genetic element, including, but not limited to, a coding region of a gene, a non-coding nucleic acid region, a regulatory element of a gene, an intron, or RNA. It is not required that the target genomic loci be associated with any specific disease, as an increase in amplifiable nucleic acid is itself diagnostic.
  • Samples typically include those generally free of intact, healthy cells, which include, but are not limited to, luminal fluid, blood (such as blood plasma or blood serum), urine, bile, pancreatic juice, stool, sputum, pus, and the like.
  • Methods of the invention can be practiced using patient samples that are most likely to contain sloughed cellular debris.
  • Such samples include, but are not limited to, stool, blood serum or plasma, sputum, pus, pancreatic fluid, bile, saliva, lymph, urine, cerebrospinal fluid, seminal fluid, and breast nipple aspirate.
  • Methods of the invention are especially useful to detect disease in biological samples comprising shed cells or cellular debris. For example, the presence in a patient stool sample of high amounts of nucleic acid, such as DNA, above a predetermined threshold is indicative that the patient has a disease, and is identified for further testing.
  • Some embodiments of the invention for use on a stool sample include obtaining a representative stool sample. Exemplary methods for preparing a stool sample are disclosed in U.S. Pat. Nos. 5,741,650 and 5,952,178, each of which is incorporated by reference herein.
  • nucleic acid being quantitatively measured by methods of the invention is DNA.
  • nucleic acids measured by the invention are not limited to any particular type of nucleic acid and include, for example, but are not limited to, total genome DNA, cDNA, RNA, mRNA, tRNA, and rRNA.
  • the nucleic acid being analyzed is selected from a coding region of a gene, or portion thereof, a noncoding nucleic acid region, or portion thereof, a regulatory element of a gene or a portion thereof, and an unidentified fragment of genomic DNA.
  • the nucleic acid being interrogated is RNA.
  • any genomic locus is amenable to screening according to the invention.
  • the particular locus or loci chosen for analysis depends, in part, on the disease being screened, and the convenience of the investigator. It is not necessary that the locus or loci chosen for analysis be correlated with any specific disease because methods of the invention contemplate measuring the amount of nucleic acid in a sample as an indicator of overall disease status.
  • disease-associated loci can be used.
  • disease-associated loci examples include p53, apc, MSH-2, dcc, scr, c-myc, B-catnenin, mlh-1, pms-1, pms-2, pol-delta, and bax.
  • the quantitative amount of amplification product may be determined by any suitable or convenient means.
  • the amount of amplification product is determined by quantitative PCR, for example, by using real-time PCR machines, such as Biorad Corporation's iCycler iQ Real Time PCR Detection System, but any quantitative system or means may be used.
  • the amplification reaction itself can be any means for amplifying nucleic acid, including, but not limited to PCR, RT-PCR, OLA, rolling circle, single base extension, and others known in the art. Methods of the invention are useful with any platform for the identification, amplification, sequencing, or other manipulation of nucleic acids.
  • methods of the invention comprise determining an amount of amplifiable nucleic acid in a biological sample, and determining whether that amount is consistent with an amount expected in a normal sample.
  • determining an amount of amplifiable nucleic acid in a biological sample and determining whether that amount is consistent with an amount expected in a normal sample.
  • the probability that any given set of PCR primers will amplify a DNA fragment having a length exceeding the primer distance is expressed as
  • FL fragment length (in base pairs) and PD is primer distance (in base pairs).
  • PD primer distance
  • Methods of the invention can be carried out by hybrid capture. For example, hybrid capture and subsequent analysis of the captured fragments can be used to determine the quantitative amount of nucleic acid in a patient sample.
  • a hybrid capture probe is used to anchor a target sequence, preferably on a solid support (e.g., beads).
  • Capture probes can be pairs of forward and reverse primers, or they can be signal amplification probes, such as those used in Ligase Chain Reaction (LCR), and others used in the identification of sequences.
  • LCR Ligase Chain Reaction
  • a sample containing a quantitative amount of nucleic acid above a predetermined threshold amount represents a positive screen according to the invention.
  • the amount of nucleic acid in a patient sample is accomplished by measuring a number of GEs in a sample.
  • One GE is equivalent to the amount of genomic DNA present in one normal cell. For example, a measurement of 100 GEs in a sample indicates that the sample contains approximately the same amount of DNA as would be found in 100 cells.
  • the number of GEs can be related to the number of copies of a particular segment of the genome, such as a particular gene, exon, or intron.
  • the number of GEs can be calculated by amplifying one or more genetic loci thought to be present in a sample and quantitatively analyzing the amount of genomic DNA in the sample through any quantitative process known in the art (for example, by comparing this amount to a known standard amount of DNA). In certain embodiments of the invention, one GE is the equivalent of about 7 picograms of DNA. In some embodiments, an amplification reaction is conducted at a single genomic locus to amplify a fragment of a specific length. Typically, fragments of 200 bp or less at the same genomic locus are amplified. There is generally a one-to-one correspondence between the amplification of a single 200 bp fragment to one genome equivalent.
  • GE scores will vary depending on a number of factors, including, but not limited to, preparation methods, amplification methods, and quantitative analysis methods, and also on the desired likelihood of false-negative results.
  • a positive screen of the invention results when the measured amount of nucleic acid in a patient sample is greater than a predetermined or threshold amount.
  • the predetermined threshold amount can be determined by amplifying a particular genetic locus in a population of normal and diseased patients.
  • the predetermined threshold amount can be determined empirically by determining the amount of nucleic acid in a sample from each of the patients in a population and setting the predetermined threshold amount based on the amount of nucleic acid in any of the patient samples (for example, below the lowest amount of nucleic acid detected in any diseased patient). Once determined, this threshold can be used as the basis for additional disease testing.
  • the threshold amount is approximately 500 GEs, although as discussed above, these scores will vary depending on a number of factors.
  • the threshold amount can be any number of GEs in the ranges of, for example, 10 to 10,000 GEs, 100 to 10,000 GEs, 200 to 8,000 GEs, 1,000 to 3,000 GEs, 1,000 to 100,000 GEs, and/or any integer between 10 and 10,000, or any range between any of two integers from 10 to 10,000.
  • the present invention provides relatively cost-effective screening methods that can be administered to a patient prior to performing additional disease testing. It should be understood that there are several ways to set a predetermined threshold amount.
  • the predetermined threshold amount can be set below either of these two numbers to reduce the likelihood of false-negative results or can be set above either of these two numbers to reduce the likelihood of false-positive results.
  • Methods of the invention are useful as screening methods. Accordingly, such methods are used to screen or to “qualify” patient samples for further analysis (e.g., genetic, biochemical, cytological, or other analyses). Often it is desirable to perform follow-up testing on a patient in order to confirm a suspected disease state. Such follow-up procedures are determined based upon the disease state being interrogated.
  • Additional disease testing of the invention includes, but is not limited to, screening assays, diagnostic evaluation, and physical examination. Additional testing of the invention includes mutation assays to detect a cancer marker (e.g., a DNA mutation) in a sample from a patient.
  • a cancer marker e.g., a DNA mutation
  • Such mutation assays include, but are not limited to, assays for the detection of mutations at the p53 tumor suppressor locus, in ras genes, in APC and DCC tumor suppressor genes, and in the BAT-26 segment of the MSH2 mismatch repair gene.
  • a mutation is a deletion, addition, substitution, rearrangement, or translocation in a nucleic acid. Numerous mutational analyses are known in the art and include, for example, U.S. Pat. No. 5,670,325, incorporated by reference herein.
  • Additional disease testing of the invention preferably comprises DNA integrity assays, as described in co-owned, co-pending U.S. patent application Ser. No. 09/455,950, incorporated by reference herein. It has been recognized that DNA obtained from exfoliated normal (non-cancerous) cells is different than DNA obtained from exfoliated cancer or precancer cells. Normal exfoliated cells typically have undergone apoptosis, and thus produce cells or cellular debris (depending upon the stage of apoptosis) comprising DNA that has been substantially degraded.
  • Exfoliated cancer or precancer cells typically have not undergone apoptosis, and such cells or their debris, while producing some very small fragments as a result of degradation in the sample, typically also contain a higher proportion of large DNA fragments (compared to those observed in cells or debris from exfoliated normal cells).
  • the difference in DNA integrity between normal and abnormal cells is a marker for the presence of cancer or precancer in a sample comprising exfoliated cells.
  • the additional disease testing component of the invention preferably comprises detecting in a biological sample one or more DNA fragment(s) of a length that would not be substantially present in noncancerous cells or cellular debris.
  • DNA fragment(s) of a length that would not be substantially present in noncancerous cells or cellular debris.
  • fragments indicative of cancer or precancer cells are between about 200 and about 3500 base pairs, and ideally between about 500 and about 2500 base pairs, such as, for example, a 1000 or 1300 base pair fragment.
  • gel electrophoresis, affinity chromatography, or mass spectrometry are used to detect large DNA fragments (fragments comprising greater than about 200 base pairs).
  • the presence of large DNA fragments in a stool sample is indicative of colorectal cancer in a patient.
  • the additional disease testing component of the invention comprises amplifying nucleic acids in a representative stool sample using human-specific primers, and detecting amplicons having greater than about 200 base pairs, and preferably about 500 or more base pairs.
  • amplification is accomplished by PCR using forward and reverse primers directed against human-specific nucleic acid-fragments, and spaced apart to provide a lower limit on the resulting amplicons.
  • the presence of amplicons greater than about 200 base pairs in length is indicative of template nucleic acid in the sample of that length (or longer). According to the additional disease testing component of the invention, such long sequences represent a positive screen and are indicative of cancer or precancer.
  • Additional testing of the invention also includes, for example, but is not limited to, performing an expression assay, a FISH assay, or an assay for enumerated LOH. Enumerated LOH assays are described in, for example, U.S. Pat. Nos. 6,203,993 and 6,300,077, each of which are incorporated by reference herein. Additional testing of the invention further includes detection of extracellular indicia of disease. Such detection methods include, for example, but are not limited to, fecal occult blood testing (FOBT) and detection of elevated antigen levels, such as carcinoembryonic or prostate-specific antigen.
  • FISH fecal occult blood testing
  • Additional testing of the invention also includes performing a diagnostic examination on a patient.
  • diagnostic examination include, but are not limited to, colonscopy, virtual colonscopy, sigmoidoscopy, flexible sigmoidoscopy, upper gastrointestinal evaluation, digital rectal examination, mammography, breast self-examination, computed tomography (CT) imaging, magnetic resonance imaging (MRI), positron emission tomography (PET), x-ray, ultrasound, biopsy, surgery, endoscopy, laparoscopy, and endoscopic retrograde cholangiopancreatography (ERCP).
  • CT computed tomography
  • MRI magnetic resonance imaging
  • PET positron emission tomography
  • ERCP endoscopic retrograde cholangiopancreatography
  • additional disease testing or follow-up analysis is used to determine where the disease resides.
  • the general disease screen is effective independent of the location of the disease and the specimen taken for analysis.
  • measurement of nucleic acid in stool is predictive of disease generally, it does not necessarily indicate that the disease is of gastrointestinal origin.
  • follow-up testing or additional disease testing are used to identify the disease.
  • Methods of the invention may be practiced in accordance with protocols for diagnosing disease in a patient.
  • the quantitative amount of nucleic acid in a sample is measured as part of a protocol for diagnosing disease in a patient.
  • FIGS. 1-5 describe particular examples of protocols for diagnosing disease in a patient.
  • the flowchart in FIG. 1 describes a basic implementation of the present invention for diagnosing disease in a patient.
  • the quantitative amount of human DNA present in a the patient sample is determined.
  • the amount of human DNA is determined as a number of GEs in the sample.
  • the patient is deemed healthy (or disease-free) in step 104 .
  • additional disease testing is performed on the patient in step 104 . This additional disease testing can be any of those described herein or any other disease testing known in the art.
  • the flowchart in FIG. 2 describes a more detailed implementation of the present invention for diagnosing disease in a patient.
  • the amount of human DNA in a sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample.
  • the amount of human DNA is lower than a predetermined threshold amount, then the patient is deemed healthy (or disease-free) in step 204 .
  • a DNA integrity test is performed on a sample from the patient in step 206 .
  • step 208 if a positive screen is obtained from the DNA integrity test, then a colonoscopy is performed on the patient in step 210 . Also at step 208 , if a negative screen is obtained from the DNA integrity test, then the patient is deemed healthy (or disease-free) in step 204 .
  • the flowchart in FIG. 3 describes a further detailed implementation of the present invention for diagnosing disease in a patient.
  • the amount of human DNA in a sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample.
  • the amount of human DNA is lower than a predetermined threshold amount, then the patient is deemed healthy (or disease-free) in step 304 . Also at step 302 , if the amount of human DNA is higher than a predetermined threshold amount, then a DNA integrity test is performed on a sample from the patient in step 306 .
  • step 308 if a positive result is obtained from the DNA integrity test, then a colonoscopy is performed on the patient in step 310 . Also at step 308 , if a negative result is obtained from the DNA integrity test, then a mutation detection assay is performed on a sample from the patient in step 312 . At step 314 , if a positive result is obtained from the mutation detection assay (i.e. a mutation is detected), then a colonoscopy is performed on the patient in step 310 . Also at step 314 , if a negative result is obtained from the mutation detection assay (i.e., a mutation is not detected), then the patient is deemed healthy (or disease-free) in step 316 .
  • the flowchart in FIG. 4 describes an even further detailed implementation of the present invention for diagnosing disease in a patient.
  • the amount of human DNA in a sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample.
  • a mutation detection assay is performed on the patient in step 404 .
  • a colonoscopy is performed on the patient in step 408 .
  • the patient is examined for symptoms of disease in step 410 .
  • step 426 If the patient is not symptomatic for disease, then the patient is deemed healthy (or disease-free) in step 426 . If the patient is symptomatic for disease, then a DNA integrity assay is performed on a sample from the patient in step 412 . At step 414 , if a positive result is obtained from the DNA integrity test, then an upper gastrointestinal work-up is performed on the patient in step 416 , followed by a colonoscopy in step 408 . Also at step 414 , if a negative result is obtained from the DNA integrity test, then the patient is deemed healthy (or disease-free) in step 426 .
  • step 402 if the amount of human DNA is higher than a predetermined threshold amount, then a DNA integrity test is performed on a sample from the patient in step 418 .
  • a DNA integrity test is performed on a sample from the patient in step 418 .
  • a colonoscopy is performed on the patient in step 408 .
  • a mutation detection assay is performed on a sample from the patient in step 422 .
  • step 424 if a positive result is obtained from the mutation detection assay, then a colonoscopy is performed on the patient in step 408 .
  • the patient is deemed healthy (or disease-free) in step 426 .
  • the flowchart in FIG. 5 describes a detailed implementation of the present invention for diagnosing colorectal cancer in a patient.
  • the amount of human DNA in a sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample.
  • a mutation detection assay is performed on the patient in step 504 .
  • a supracolonic work-up is performed on the patient in step 508 .
  • a negative result is obtained from the mutation detection assay, then the patient is deemed healthy in step 510 .
  • step 502 if the amount of human DNA is higher than a predetermined threshold amount, then a DNA integrity test is performed on a sample from the patient in step 512 .
  • a DNA integrity test is performed on a sample from the patient in step 512 .
  • a colonoscopy is performed on the patient in step 516 .
  • a mutation detection assay is performed on a sample from the patient in step 518 .
  • step 520 if a positive result is obtained from the mutation detection assay, then a colonoscopy is performed on the patient in step 516 . Also at step 520 , if a negative result is obtained from the mutation detection assay, then the patient is deemed healthy in step 510 .
  • the present invention provides relatively cost-effective screening methods that can be administered to a patient prior to performing additional disease testing.
  • Methods of the invention are useful as general disease screening techniques, and are useful as screens for a wide-range of disease states.
  • Methods of the inventions are also useful as screening techniques for the presence of cancer and pre-cancer, and are especially useful as screening techniques colorectal cancer and pre-cancer.
  • methods of the invention are useful to screen for other cancers, for example, as screening techniques for lymphomas, stomach cancers, lung cancers, liver cancers, pancreas cancers, prostrate cancers, kidney cancers, testicular cancers bladder cancers, gallbladder cancers, uterine cancers, and ovarian cancers.
  • Methods of the invention are also useful for screening for the presence of cancerous or precancerous lesions in a patient, including adenomas.
  • methods of the invention are useful, for example, as screening techniques for diseases such as inflammatory bowel syndrome, inflammatory bowel disease, Crohn's disease, respiratory distress syndrome, and others in which the performance of diagnostic procedures followed by the performance of screening methods of the invention would be effective in the detection of disease.
  • the methods of the invention are also useful for detecting an indicator of the presence of an infectious agent, including, but not limited to, a virus, bacterium, parasite, or other microorganism.
  • infectious agent including, but not limited to, a virus, bacterium, parasite, or other microorganism.
  • the invention is equally applicable to human and to veterinary uses. Accordingly, “patient” as discussed herein is intended to included humans and other animals.
  • methods of the invention are used to monitor the progress of a disease in a patient or in populations of patients.
  • Such longitudinal monitoring provides information on the degree to which the quantitative amount of nucleic acid in samples is increasing or decreasing as disease progresses or recedes.
  • Longitudinal monitoring of the total genomic DNA in a patient sample can be done without reference to an external predetermined threshold and, instead, uses amounts determined at prior time point(s) as the predetermined threshold.
  • the nucleic acid in a patient's sample can be quantified at two or more time points. If the amount of nucleic acid increases from one or more previous time points, the patient can be tested with follow up additional disease testing.
  • the amount of nucleic acid in a patient's sample can be quantified at two or more time points, and, if the amount of nucleic acid decreases from one or more previous time points and if the patient is being treated for a disease, the patient may show signs of partial or total abatement, alleviation, or treatment of a disease.
  • longitudinal monitoring can be used to assess the efficacy of treatments (e.g., chemotherapy, antibiotics), and the response of patients to therapeutic interventions.
  • Methods of the invention can also be used to predict disease flare-up. For example, monitoring fluctuations in the quantitative amount of nucleic acids in samples from diseased patients, such as patients with inflammatory bowel disease, is useful to predict onset of disease episodes. According to the invention, episodic occurrence of symptoms is tied to an increase in the quantitative amount of nucleic acids in patient samples.
  • Methods of the invention are also useful to establish patient databases. Such databases are used to identify specific patients, to establish where a particular patient fits in a disease continuum, to follow trends in disease, to predict disease onset, or to compile statistics on disease frequency, to monitor patient progress and treatment efficacy, and the like.
  • Methods of the invention are also useful to predict risk for disease and to predict disease onset.
  • Levels of nucleic acids in patient samples are useful as a quantitative or quasi-quantitative measure of disease.
  • the level of, for example, nucleic acids obtained from a patient sample is compared to predetermined threshold amounts representing various stages of disease in order to assess the patient's disease state and prognosis.
  • methods of the invention were correlated with the clinical outcome in 49 patients who were previously diagnosed (using colonoscopy) as having colorectal cancer, and 100 patients who were diagnosed as not having colorectal cancer.
  • the threshold amount (the amount at which patients below such amount can be identified as being relatively disease-free) for use in methods of the invention was empirically determined as described below.
  • Stool specimens were collected from patients and frozen. Each frozen stool specimen, weighing approximately 32 grams, was thawed and homogenized in buffer.
  • the buffer was comprised of 0.5 M Tris, 10 mM NaCl, and 150 mM EDTA, essentially as disclosed in U.S. Pat. No. 6,551,777, incorporated by reference herein. Each of the samples was then diluted with additional buffer (not containing EDTA) to a final buffer to stool ratio of 20:1.
  • Each sample was centrifuged, and the supernatant, which carried the active DNA degrading fraction, was removed to a clean tube. The supernatant was collected and treated with sodium dodecyl sulfate and Proteinase K.
  • the DNA in each sample was then prepared by standard techniques. See, e.g., Ausubel et al., Short Protocols in Molecular Biology ⁇ 2.1-2.4 (3d ed. 1995). A phenol extraction, a phenol/chloroform extraction, and a phenol extraction were performed prior to isolating the DNA. The isolated DNA was then placed into a standard. Tris buffer.
  • the DNA samples were amplified using quantitative PCR.
  • a PCR primer set from Midland Certified Reagent Company, TaqMan® probes from PanVera Corporation and a real-time PCR instrument were used (Biorad Corporations's iCycler iQ Real Time PCR Detection System).
  • TaqMan® analysis was performed on an ABI 7700 thermalcycler (Applied Biosystems, Foster City, Calif.) using primers against a 200 base pair region of the APC gene.
  • the 5′ primer was: 5′AGCCCCAGTGATCTTCCAGAT3′ (SEQ ID NO: 1).
  • the ′3 primer was: 5′AGGTGGTGGAGGTGTTTTACTTCT3′ (SEQ ID NO: 2).
  • a FAM/TAMRA probe was used to detect amplified PCR product: FAM-CCCTGGACAAACCATGCCACCAA-TAMRA (SEQ ID NO: 3).
  • Amplification reactions consisted of captured human stool DNA mixed with TaqMan® PCR Universal Master mix (Applied Biosystems, Foster City, Calif.), 1 ⁇ PCR primers (5 ⁇ mol/L), and 1 ⁇ TaqMan® probe (2 ⁇ mol/L) (Applied Biosystems, Foster City, Calif.). 5 mls of captured DNA were used in PCR reactions.
  • TaqMan® reactions were performed as follows. Thermal cycling began with a primer annealing step (50° C. for 2 min) and one cycle of DNA denaturation (95° C. for 10 minutes). This was followed by 40 cycles of sequential DNA denaturation (95° C. for 1 min) and primer annealing (60° C. for 1 min).
  • the ABI 7700 unit detected amplification products with the FAM/TAMRA probe and data used in the calculation of genome equivalents per reaction was provided. Clinical status was determined by performing a colonoscopy on each patient. The results are shown in the Table 1 below. TABLE 1 Patient No.
  • the diagnoses of “normal” or “minor polyps” are considered “normal patients” as discussed herein.
  • the diagnoses of “Dukes A,” “Dukes B,” “Dukes C” refer to the stages of colorectal cancer), “LGD” (Low Grade Dysplasia), “HGD” (High Grade Dysplasia), and “CIS” (Carcinoma In Situ) are considered “cancer patients” as discussed herein.
  • the predetermined threshold amount for use in methods of the invention can be set to any score below 652.
  • the GE score can be set at 650. Based on this score, 17% of normal patients would not have to undergo additional disease testing.
  • the GE score can be set at 630 (i.e., the highest number of GEs for a normal patient that is less than the lowest number of GEs for a cancer patient).
  • the GE score can be set at 500 to eliminate potential false-negatives in future testing. Based on this score, 14% of normal patients would not have to undergo additional disease testing. As another example, the GE score can be set at 250. Based on this score, 9% of normal patients would not have to undergo additional disease testing. As a further example, the GE score can be set at 200. Based on this score, 5% of normal patients would not have to undergo additional disease testing. As a further example, the GE score can be set at 700 to eliminate potential false-positives in future testing.
  • a subset of the patient population would not have to undergo additional disease testing based on GE scores below the predetermined threshold amount.
  • the same preparation methods, amplification methods, and quantitative analysis methods that were used to determined the threshold amount should be used when screening patient samples in accordance with the invention.
  • the patient is identified as a candidate for additional disease testing. For example, if the predetermined threshold amount is 1,000 GEs, and a patient sample measures 50,000 GEs, then the patient would be a candidate for additional disease testing.
  • Example 3 describes another preferred method of additional disease testing in accordance with the invention.
  • Detection of DNA fragments of at least 200 base pairs in length are also useful in an additional disease testing phase of the invention, as the amount of 200 bp or greater DNA in a sample is predictive of cancer or precancer in patients.
  • the samples are screened by hybrid capturing human DNA and determining the amount of amplifiable DNA having at least 200 base pairs. Stool samples are prepared as described in Example 1.
  • Human DNA is isolated from stool precipitate by sequence-specific hybrid capture. Biotynilated probes against portions of the p53, K-ras, and ape genes are used.
  • the K-ras probe is 5′GTGGAGTATTTGATAGTGTATTAACCTTATGTGTGAC 3′ (SEQ ID NO: 4).
  • the apc-1309 probe is 5′TTCCAGCAGTGTCACAGCACCCTAGAACCAAATCCAG 3′ (SEQ ID NO: 5)
  • the apc-1378 probe is 5′CAGATAGCCCTGGACAAACAATGCCACGAAGCAGAAG 3′ (SEQ ID NO: 6).
  • the first (hybridizing to a portion of exon 5) is 5′TACTCCCCTGCCCTCAACAAGATGTTTTGCCAACTGG3′ (SEQ ID NO: 7)
  • the second (hybridizing to a portion of exon 7) is 5′ATTTCTTCCATACTACTACCCATCGACCTCTCATC3′ (SEQ ID NO: 8)
  • the third, also hybridizing to a portion of exon 7 is 5′ATGAGGCCAGTGCGCCTTGGGGAGACCTGTGGCAAGC3′ (SEQ ID NO: 9)
  • a probe against exon 8 has the sequence 5′GAAAGGACAAGGGTGGTTGGGAGTAGATGGAGCCTGG3′ (SEQ ID NO: 10).
  • a 10 ⁇ l aliquot of each probe (20 pmol/capture) is added to a suspension containing 300 ⁇ l DNA in the presence of 310 ⁇ l 6M GITC buffer for 2 hours at room temperature.
  • Hybrid complexes are isolated using streptavidin-coated beads (Dynal). After washing, probe-bead complexes are suspended at 25° C. for 1 hour in 0.1 ⁇ TE buffer, pH7.4. The suspension is then heated for 4 minutes at 85° C., and the beads are removed.
  • Each sample is amplified using forward and reverse primers through 7 loci (Kras, exon 1, APC exon 15 (3 separate loci), p53, exon 5, p53, exon 7, and p53, exon 8) in duplicate (for a total of 14 amplifications for each locus). Seven separate PCRs (33 cycles each) are run in duplicate using primers directed to detect fragments in the sample having 200 base pairs or more.
  • Amplified DNA is placed on a 4% Nusieve (FMC Biochemical) gel (3% Nusieve, 1% agarose), and stained with ethidium bromide (0.5 ⁇ g/ml). The resulting amplified DNA is graded based upon the relative intensity of the stained gels.
  • Samples from a patient with cancer or adenoma are detected as a band having significantly greater intensity than the bands associated with samples from patients who do not have cancer or precancer. Patients are identified as having cancer or adenoma by determining the amount of amplifiable DNA measuring 200 base pairs or greater in length.
  • the patient if the amount of DNA in a patient sample is greater than the predetermined threshold amount, then the patient is identified as a candidate for additional disease testing. For example, if the predetermined threshold amount is 500 GEs, and a patient sample measures 20,000 GEs, then the patient would be a candidate for additional disease testing.
  • Example 2 describes a preferred method of additional disease testing in accordance with the invention.
  • the BAT-26 segment of the MSH1 mismatch repair locus (shown in SEQ ID NO: 11) is useful in the additional disease testing phase of the invention, as-deletions in BAT-26 have been associated with colorectal cancer. Stool samples are prepared as described in Example 1.
  • a primer is hybridized to the portion of the BAT-26 locus immediately upstream of the poly-A tract, which consists of 26 adenosines (nucleotides 195-221). Unlabeled deoxythymidine, a mixture of labeled and unlabeled deoxycytosine, and unlabeled dideoxyadenine are added along with polymerase. The primer is extended through the poly-A region. The labeled and unlabelled cytosine is extended for the next three bases (nucleotides 222-224, all guanines in the intact sequence) such that label is incorporated into each extended primer. After the poly-A tract and the three guanines, there exist two thymidines in the intact sequence.
  • the dideoxyadenosine stops primer extension by addition at the end of a primer that is extended through the poly-A and triguanine regions. Strands are separated, and the length of the strands are observed on a polyacrylamide gel to detect deletions in the poly-A tract. Deletions in the poly-A tract are indicative of colorectal cancer.

Abstract

Methods of the invention generally include measuring a quantitative amount of nucleic acid in a patient sample, and optionally, performing additional disease testing on the patient. Methods of the invention are useful in screening disease in a patient, such as cancer.

Description

    FIELD OF THE INVENTION
  • This invention generally relates to methods for screening for disease in a patient. More specifically, this invention relates to the quantitative analysis of nucleic acids in a patient sample, and optionally, performing additional disease testing. [0001]
  • BACKGROUND OF THE INVENTION
  • Current methods of disease screening involve examining or testing individuals for early stages of disease. Preferably, individuals are screened for disease even before they exhibit symptoms. Early-stage screening is important because early diagnosis of a disease can make treatment easier and more effective, and can decrease mortality. Additionally, early treatment of a disease may help to slow, stop, or even reverse disease progression so that an individual never becomes symptomatic. [0002]
  • Current disease screening methods include, for example, invasive tests and cellular-based assays. Examples of invasive tests include physical examination and biopsy of potentially-cancerous tissue. Examples of cellular-based assays include analysis of DNA, RNA, chromosomes, proteins, and certain metabolites to detect heritable disease-related genotypes, mutations, phenotypes, or karyotypes for clinical purposes. Genetic assays for cancer often involve probing specific genes for previously identified mutations. For example, a number of genetic mutations, including alterations in the BAT-26 segment of the MSH2 mismatch repair gene, the p53 gene, the ras oncogene, and the APC tumor suppressor gene have been associated with the multi-step pathway leading to cancer. [0003]
  • Known screening methods contain a number of practical limitations. For example, invasive cancer screening procedures are often expensive and can result in significant patient discomfort or possibly severe medical complications. Further, the cost of commercially available genetic assays for disease screening can range from hundreds to thousands of dollars, depending on the sizes of the genes and the numbers of mutations tested. Accordingly, there is a need in the art for relatively simple and inexpensive screening methods that can be administered to a patient prior to performing additional disease testing. Such methods are provided herein. [0004]
  • SUMMARY OF THE INVENTION
  • The present invention is based on the observation that the amount of nucleic acid in a patient sample is indicative of the presence of disease in the patient. Accordingly, methods of the invention comprise quantifying an amount of nucleic acid in a patient sample. If the amount of nucleic acid in the sample is greater than a predetermined threshold amount, then the patient is identified as a candidate for additional disease testing. The predetermined threshold amount is preferably set so that patient samples having an amount of nucleic acid lower than the predetermined threshold amount can be identified as being relatively disease-free. Methods of the invention are useful as screening techniques for any disease, including cancer, such as, but not limited to, colorectal cancer. [0005]
  • Methods of the invention can be used to identify a subset of a patients in a population that are relatively disease-free. In certain embodiments, this patient subset does not undergo additional disease testing, although additional disease testing may be performed if desired. In one embodiment, the predetermined threshold amount is set so that approximately 10-20% of patients in a population can be identified as being relatively disease-free using methods of the invention. Therefore, the present invention provides cost-effective screening methods to determine if a patient is a candidate for additional disease testing. [0006]
  • Methods of the invention provide that the quantitative amount of nucleic acid in a sample is indicative of disease status of the patient from whom the sample was obtained. According to the invention, tissue or body fluid samples, especially those described below, contain shed cellular debris. In diseases such as cancer in which cells undergo uncontrolled cell growth and the cell cycle mechanisms are destroyed or impaired, it is believed (without any intention of being bound by the theory) that samples containing cellular debris from such patients have an increased amount of nucleic acid relative to samples from certain healthy patients. As a result, it has been discovered that patients can be screened for disease by quantitatively measuring an amount of nucleic acid in a patient sample. [0007]
  • Methods of the invention are practiced by quantifying an amount of nucleic acid in a sample and comparing the measured amount to a predetermined threshold amount. A positive screen represents a measured amount of nucleic acid greater than the predetermined threshold amount. A negative screen represents a measured amount of nucleic acid lower than the predetermined threshold amount. [0008]
  • The predetermined threshold amount can be determined by empirical means. For example, the predetermined threshold amount can be determined by amplifying a particular genetic locus in a sample from each of a population of normal and diseased patients and quantitatively analyzing the amount of DNA in each of the patients in the population. The predetermined threshold amount is preferably set below the measured amount of nucleic acid in any of the diseased patient samples. Once the predetermined threshold amount has been determined, it can be used as the basis for further screening. [0009]
  • There are numerous ways in which the amount of nucleic acid in a patient sample is quantitatively measured. In certain embodiments, the amount of nucleic acid in a patient sample is quantitatively measured by calculating a number of genome equivalents (as used herein, genome equivalents is abbreviated “GE”) in a sample. For example, one GE is equivalent to the amount of genomic DNA present in one normal cell. Thus, as one non-limiting example, a measurement of 100 GEs in a sample indicates that the sample contains approximately the same amount of DNA as would be found in 100 cells. In certain circumstances, the number of GEs can be related to the number of copies of a particular segment of the genome, such as a particular gene, exon, or intron. The number of GEs can be calculated by amplifying one or more genetic loci thought to be present in a sample and quantitatively analyzing the amount of genomic DNA in the sample through any quantitative process known in the art. In certain embodiments of the invention, one GE is the equivalent of about 7 picograms of DNA. In some embodiments, an amplification reaction is conducted at a single genomic locus to amplify a fragment of a specific length. Typically, fragments of 200 bp or less at the same genomic locus are amplified. There is generally a one-to-one correspondence between the amplification of a single 200 bp fragment and one genome equivalent. Therefore, quantitative PCR will determine how many 200 bp fragments of a specific site were available originally in the sample, and thus, the number of GEs in the sample. GE scores will vary depending on a number of factors, including, but not limited to, preparation methods, amplification methods, and quantitative analysis methods. In certain embodiments, the quantity of human genomic DNA (or other patient DNA, such as animal DNA) in a heterogeneous sample comprising shed cells or cellular debris is measured. [0010]
  • Additional disease testing of the invention includes, but is not limited to, genetic assays, diagnostic evaluation, and physical examination. Methods of the invention are useful as general disease screening techniques, and are useful as screens for a wide-range of disease states. Methods of the inventions are also useful as screening techniques for the presence of cancer and pre-cancer, and are especially useful as screening techniques for colorectal cancer and pre-cancer. [0011]
  • In one aspect of the invention, the invention provides methods for screening a patient for the presence of disease including the steps of measuring a quantitative amount of nucleic acid in a patient sample comprising shed cells or cellular debris, and identifying the patient as a candidate for additional disease testing if the amount of nucleic acid is above a predetermined threshold amount. [0012]
  • This aspect of the invention can have any of the following features. The nucleic acid can be genomic DNA. The measuring step can include determining a number of genome equivalents. The method can further include the step of performing an assay on a sample from the patient if the patient is identified as a candidate for additional disease testing. This assay can be a DNA integrity assay, mutation detection assay, enumerated loss of heterozygosity (LOH) assay, expression assay, and/or fluorescent in-situ hybridization (FISH) assay. The assay can detect mutations at any genetic locus such as, but not limited to, p53, ras, APC, DCC, and/or BAT-26. The method can further include the step of performing a diagnostic examination on the patient if the patient is identified as a candidate for additional disease testing. The step of performing a diagnostic examination can be a colonoscopy, a sigmoidoscopy, a fecal occult blood testing and/or an upper gastrointestinal evaluation. The patient sample can be stool, sputum, pancreatic fluid, bile, lymph, blood (such as blood serum or blood plasma), urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and/or pus. The disease can be cancer or pre-cancer. The cancer can be colorectal cancer, lung cancer, esophageal cancer, prostrate cancer, stomach cancer, pancreatic cancer, liver cancer, and/or lymphoma. [0013]
  • In another aspect of the invention, the invention provides methods for screening a patient for the presence of abnormal proliferating cells including the steps of measuring a quantitative amount of nucleic acid in a patient sample including shed cells or cellular debris, and identifying a positive screen as a sample in which the amount of nucleic acid is above a predetermined threshold amount. [0014]
  • This aspect of the invention can include any of the features described above or below. The nucleic acid can be genomic DNA. The measuring can be determining a number of genomic equivalents. The method can further include the step of performing an assay on a sample from the patient if a positive screen is identified in the identifying step. This assay can be a DNA integrity assay, mutation detection, enumerated LOH, expression assays, and FISH. This assay also can be one that detects mutations at a genetic locus including p53, ras, APC, DCC, and/or BAT-26. The method can further include the step of performing a diagnostic examination on the patient if a positive screen is identified in the identifying step. The step of performing a diagnostic examination can be a colonoscopy, a sigmoidoscopy, a fecal occult blood testing and/or an upper gastrointestinal evaluation. The patient sample can be stool, sputum, pancreatic fluid, bile, lymph, blood (such as blood serum or blood plasma), urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and/or pus. [0015]
  • In a further aspect of the invention, the invention provides methods for diagnosing the state of health of a patient including the steps of measuring a quantitative amount of nucleic acid in a patient sample including shed cells or cellular debris, and performing an assay on a sample from the patient if the amount of nucleic acid is above a predetermined threshold amount such that the state of health of a patient is determined. [0016]
  • This aspect of the invention can have any of the following or preceding features. The nucleic acid can be genomic DNA. The measuring can include determining a number of genome equivalents. The assay can be a DNA integrity assay, mutation detection, enumerated LOH, expression assays, and/or FISH. The assay can detect mutations at a genetic locus including p53, ras, APC, DCC, and/or BAT-26. The method can further include performing a diagnostic examination on the patient. The diagnostic examination can be a colonoscopy, a sigmoidoscopy, a fecal occult blood testing, and/or an upper gastrointestinal evaluation. The patient sample can be stool, sputum, pancreatic fluid, bile, lymph, blood (such as blood serum or blood plasma), urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and/or pus. [0017]
  • The present invention is pointed out with particularity in the appended claims. The objects and advantages of the invention described above, as well as further objects and advantages of the invention, are better understood by reference to the following detailed description taken in conjunction with the accompanying drawings.[0018]
  • DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a flowchart representation of method steps for diagnosing disease in a patient in accordance with one embodiment of the invention. [0019]
  • FIG. 2 is a flowchart representation of method steps for diagnosing disease in a patient in accordance with another embodiment of the invention. [0020]
  • FIG. 3 is a flowchart representation of method steps for diagnosing disease in a patient in accordance with a further embodiment of the invention. [0021]
  • FIG. 4 is a flowchart representation of method steps for diagnosing disease in a patient in accordance with another embodiment of the invention. [0022]
  • FIG. 5 is a flowchart representation of method steps for diagnosing colorectal cancer in accordance with one particular embodiment of the invention.[0023]
  • DETAILED DESCRIPTION OF THE INVENTION
  • Methods of the present invention are useful in screening for disease in a patient. Methods of the invention provide that the amount of nucleic acid in a sample comprising shed cellular material is indicative of the disease status of the patient from whom the sample was obtained. In general, methods of the invention comprise measuring the quantitative amount of nucleic acid in a sample from a patient. If the measured amount of nucleic acid in the sample is greater than a predetermined threshold amount, then additional disease testing is performed on the patient. The additional disease testing includes, for example, genetic assays and physical examination. If the measured amount of nucleic acid in the sample is lower than a predetermined threshold amount, then no additional disease testing is necessary, although it can be conducted if desired. Accordingly, the present invention provides relatively cost-effective screening methods that can be administered to a patient prior to performing additional disease testing on the patient. [0024]
  • As discussed herein, the present invention is based on the observation that the amount of nucleic acids in a patient sample is indicative of the presence of disease. In one embodiment, methods of the invention comprise screening a patient sample by conducting an amplification reaction using as a template a nucleic acid suspected or expected to be in the sample; measuring a quantitative amount of amplification product obtained; comparing the amount of amplification product obtained to a predetermined threshold amount; and identifying the patient as a candidate for additional disease testing if the amount of amplification product is greater than the predetermined threshold amount. In certain embodiments, a predetermined threshold amount is determined by empirical means. Also in certain embodiments, a predetermined threshold amount is determined by reference to the art. [0025]
  • One method of the invention includes conducting in a tissue or body fluid sample an amplification reaction using as a template a nucleic acid locus suspected to be in the sample. If the amount of amplification product (amplicon) is greater than a predetermined threshold amount, then additional testing may be performed on a patient. In the case of DNA, the amplification reaction can be a polymerase chain reaction (PCR). Methods for conducting PCR are provided in U.S. Pat. No. 4,683,202, incorporated by reference herein. In the case of RNA, the amplification reaction can be reverse transcriptase PCR. Primers are designed to amplify the locus or loci chosen for analysis. For purposes of the invention a “genomic locus” is any genetic element, including, but not limited to, a coding region of a gene, a non-coding nucleic acid region, a regulatory element of a gene, an intron, or RNA. It is not required that the target genomic loci be associated with any specific disease, as an increase in amplifiable nucleic acid is itself diagnostic. [0026]
  • Any tissue or body fluid specimen may be used as a patient sample according to methods of the invention. Samples typically include those generally free of intact, healthy cells, which include, but are not limited to, luminal fluid, blood (such as blood plasma or blood serum), urine, bile, pancreatic juice, stool, sputum, pus, and the like. Methods of the invention can be practiced using patient samples that are most likely to contain sloughed cellular debris. Such samples include, but are not limited to, stool, blood serum or plasma, sputum, pus, pancreatic fluid, bile, saliva, lymph, urine, cerebrospinal fluid, seminal fluid, and breast nipple aspirate. Methods of the invention are especially useful to detect disease in biological samples comprising shed cells or cellular debris. For example, the presence in a patient stool sample of high amounts of nucleic acid, such as DNA, above a predetermined threshold is indicative that the patient has a disease, and is identified for further testing. Some embodiments of the invention for use on a stool sample include obtaining a representative stool sample. Exemplary methods for preparing a stool sample are disclosed in U.S. Pat. Nos. 5,741,650 and 5,952,178, each of which is incorporated by reference herein. [0027]
  • Methods of the invention are practiced by measuring the quantitative amount of nucleic acids in a patient sample. In certain embodiments, the nucleic acid being quantitatively measured by methods of the invention is DNA. However, nucleic acids measured by the invention are not limited to any particular type of nucleic acid and include, for example, but are not limited to, total genome DNA, cDNA, RNA, mRNA, tRNA, and rRNA. In a particular embodiment, the nucleic acid being analyzed is selected from a coding region of a gene, or portion thereof, a noncoding nucleic acid region, or portion thereof, a regulatory element of a gene or a portion thereof, and an unidentified fragment of genomic DNA. Also in certain embodiments, the nucleic acid being interrogated is RNA. As is appreciated by the skilled artisan, any genomic locus is amenable to screening according to the invention. The particular locus or loci chosen for analysis depends, in part, on the disease being screened, and the convenience of the investigator. It is not necessary that the locus or loci chosen for analysis be correlated with any specific disease because methods of the invention contemplate measuring the amount of nucleic acid in a sample as an indicator of overall disease status. However, disease-associated loci (those in which a mutation is indicative, causative, or otherwise evidences a disease) can be used. Examples of disease-associated loci include p53, apc, MSH-2, dcc, scr, c-myc, B-catnenin, mlh-1, pms-1, pms-2, pol-delta, and bax. [0028]
  • The quantitative amount of amplification product may be determined by any suitable or convenient means. Preferably, the amount of amplification product is determined by quantitative PCR, for example, by using real-time PCR machines, such as Biorad Corporation's iCycler iQ Real Time PCR Detection System, but any quantitative system or means may be used. The amplification reaction itself can be any means for amplifying nucleic acid, including, but not limited to PCR, RT-PCR, OLA, rolling circle, single base extension, and others known in the art. Methods of the invention are useful with any platform for the identification, amplification, sequencing, or other manipulation of nucleic acids. [0029]
  • In certain embodiments, methods of the invention comprise determining an amount of amplifiable nucleic acid in a biological sample, and determining whether that amount is consistent with an amount expected in a normal sample. In many biological samples, especially heterogeneous samples, there may be no detectable amplification product. That is especially true when longer fragments are used as templates for amplification. Generally, the probability that any given set of PCR primers will amplify a DNA fragment having a length exceeding the primer distance is expressed as [0030]
  • % of Fragments Amplified=(FL−PD)/(FL+PD)
  • wherein FL is fragment length (in base pairs) and PD is primer distance (in base pairs). This equation assumes that sample DNA fragment lengths are uniformly distributed (i.e., there is no favored locus at which breaks occur). The lengths of fragments to be amplified in this assay may be varied, but are preferably less than 200 bp in length. [0031]
  • Methods of the invention can be carried out by hybrid capture. For example, hybrid capture and subsequent analysis of the captured fragments can be used to determine the quantitative amount of nucleic acid in a patient sample. In certain embodiments, a hybrid capture probe is used to anchor a target sequence, preferably on a solid support (e.g., beads). Capture probes can be pairs of forward and reverse primers, or they can be signal amplification probes, such as those used in Ligase Chain Reaction (LCR), and others used in the identification of sequences. The probes hybridize along the target fragment. Thus, by analyzing samples for the presence of the probes, one can determine the quantitative amount of nucleic acid present in the sample. This can be done in numerous ways, including, but not limited to, hybrid capture, PCR, LCR, strand displacement, branched chain, or other assays known in the art that incorporate hybrid probes or primers to quantitate a sequence. A sample containing a quantitative amount of nucleic acid above a predetermined threshold amount represents a positive screen according to the invention. [0032]
  • There are numerous ways in which the quantitative amount of nucleic acid in a sample is calculated. In certain embodiments, the amount of nucleic acid in a patient sample is accomplished by measuring a number of GEs in a sample. One GE is equivalent to the amount of genomic DNA present in one normal cell. For example, a measurement of 100 GEs in a sample indicates that the sample contains approximately the same amount of DNA as would be found in 100 cells. In certain circumstances, the number of GEs can be related to the number of copies of a particular segment of the genome, such as a particular gene, exon, or intron. The number of GEs can be calculated by amplifying one or more genetic loci thought to be present in a sample and quantitatively analyzing the amount of genomic DNA in the sample through any quantitative process known in the art (for example, by comparing this amount to a known standard amount of DNA). In certain embodiments of the invention, one GE is the equivalent of about 7 picograms of DNA. In some embodiments, an amplification reaction is conducted at a single genomic locus to amplify a fragment of a specific length. Typically, fragments of 200 bp or less at the same genomic locus are amplified. There is generally a one-to-one correspondence between the amplification of a single 200 bp fragment to one genome equivalent. Therefore, quantitative PCR will determine how many 200 bp fragments of a specific site were available originally in the sample, and thus, the number of GEs in the sample. GE scores will vary depending on a number of factors, including, but not limited to, preparation methods, amplification methods, and quantitative analysis methods, and also on the desired likelihood of false-negative results. [0033]
  • A positive screen of the invention results when the measured amount of nucleic acid in a patient sample is greater than a predetermined or threshold amount. In one embodiment, the predetermined threshold amount can be determined by amplifying a particular genetic locus in a population of normal and diseased patients. The predetermined threshold amount can be determined empirically by determining the amount of nucleic acid in a sample from each of the patients in a population and setting the predetermined threshold amount based on the amount of nucleic acid in any of the patient samples (for example, below the lowest amount of nucleic acid detected in any diseased patient). Once determined, this threshold can be used as the basis for additional disease testing. In one particular embodiment of the invention, the threshold amount is approximately 500 GEs, although as discussed above, these scores will vary depending on a number of factors. By way of further examples, and without any intent of limiting the scope of the invention to such examples, the threshold amount can be any number of GEs in the ranges of, for example, 10 to 10,000 GEs, 100 to 10,000 GEs, 200 to 8,000 GEs, 1,000 to 3,000 GEs, 1,000 to 100,000 GEs, and/or any integer between 10 and 10,000, or any range between any of two integers from 10 to 10,000. [0034]
  • In accordance with the invention, if the amount of nucleic acid in the patient sample is greater than the predetermined threshold amount, then the patient is identified as a candidate for additional disease testing. If the amount of nucleic acid in the sample is lower than the predetermined or threshold amount, then no additional disease testing is necessary, although such testing may be performed if desired. As such, the present invention provides relatively cost-effective screening methods that can be administered to a patient prior to performing additional disease testing. It should be understood that there are several ways to set a predetermined threshold amount. For example, one can set the threshold below the amount of nucleic acid (e.g., GEs) in a sample from the diseased patient exhibiting the lowest amount of nucleic acid in a group of patients (both normal and diseased) or below the amount of nucleic acid in a sample from the normal patient exhibiting the highest amount of genomic DNA that is not greater than the amount of nucleic acid of the diseased patient exhibiting the lowest amount of nucleic acid in a group of patients. Moreover, the predetermined threshold amount can be set below either of these two numbers to reduce the likelihood of false-negative results or can be set above either of these two numbers to reduce the likelihood of false-positive results. [0035]
  • Methods of the invention are useful as screening methods. Accordingly, such methods are used to screen or to “qualify” patient samples for further analysis (e.g., genetic, biochemical, cytological, or other analyses). Often it is desirable to perform follow-up testing on a patient in order to confirm a suspected disease state. Such follow-up procedures are determined based upon the disease state being interrogated. [0036]
  • Additional disease testing of the invention includes, but is not limited to, screening assays, diagnostic evaluation, and physical examination. Additional testing of the invention includes mutation assays to detect a cancer marker (e.g., a DNA mutation) in a sample from a patient. Such mutation assays include, but are not limited to, assays for the detection of mutations at the p53 tumor suppressor locus, in ras genes, in APC and DCC tumor suppressor genes, and in the BAT-26 segment of the MSH2 mismatch repair gene. For purposes of the present invention, a mutation is a deletion, addition, substitution, rearrangement, or translocation in a nucleic acid. Numerous mutational analyses are known in the art and include, for example, U.S. Pat. No. 5,670,325, incorporated by reference herein. [0037]
  • Additional disease testing of the invention preferably comprises DNA integrity assays, as described in co-owned, co-pending U.S. patent application Ser. No. 09/455,950, incorporated by reference herein. It has been recognized that DNA obtained from exfoliated normal (non-cancerous) cells is different than DNA obtained from exfoliated cancer or precancer cells. Normal exfoliated cells typically have undergone apoptosis, and thus produce cells or cellular debris (depending upon the stage of apoptosis) comprising DNA that has been substantially degraded. Exfoliated cancer or precancer cells typically have not undergone apoptosis, and such cells or their debris, while producing some very small fragments as a result of degradation in the sample, typically also contain a higher proportion of large DNA fragments (compared to those observed in cells or debris from exfoliated normal cells). The difference in DNA integrity between normal and abnormal cells is a marker for the presence of cancer or precancer in a sample comprising exfoliated cells. [0038]
  • In one embodiment, the additional disease testing component of the invention preferably comprises detecting in a biological sample one or more DNA fragment(s) of a length that would not be substantially present in noncancerous cells or cellular debris. There is no upper limit on these fragments, as all that is necessary is that the fragment be larger than an apoptotic fragment (i.e., about 200 bp). Typically, however, fragments indicative of cancer or precancer cells are between about 200 and about 3500 base pairs, and ideally between about 500 and about 2500 base pairs, such as, for example, a 1000 or 1300 base pair fragment. In certain embodiments, gel electrophoresis, affinity chromatography, or mass spectrometry are used to detect large DNA fragments (fragments comprising greater than about 200 base pairs). In one embodiment, the presence of large DNA fragments in a stool sample is indicative of colorectal cancer in a patient. [0039]
  • In certain embodiments, the additional disease testing component of the invention comprises amplifying nucleic acids in a representative stool sample using human-specific primers, and detecting amplicons having greater than about 200 base pairs, and preferably about 500 or more base pairs. In certain embodiments, amplification is accomplished by PCR using forward and reverse primers directed against human-specific nucleic acid-fragments, and spaced apart to provide a lower limit on the resulting amplicons. The presence of amplicons greater than about 200 base pairs in length is indicative of template nucleic acid in the sample of that length (or longer). According to the additional disease testing component of the invention, such long sequences represent a positive screen and are indicative of cancer or precancer. [0040]
  • Additional testing of the invention also includes, for example, but is not limited to, performing an expression assay, a FISH assay, or an assay for enumerated LOH. Enumerated LOH assays are described in, for example, U.S. Pat. Nos. 6,203,993 and 6,300,077, each of which are incorporated by reference herein. Additional testing of the invention further includes detection of extracellular indicia of disease. Such detection methods include, for example, but are not limited to, fecal occult blood testing (FOBT) and detection of elevated antigen levels, such as carcinoembryonic or prostate-specific antigen. [0041]
  • Additional testing of the invention also includes performing a diagnostic examination on a patient. Examples of diagnostic examination include, but are not limited to, colonscopy, virtual colonscopy, sigmoidoscopy, flexible sigmoidoscopy, upper gastrointestinal evaluation, digital rectal examination, mammography, breast self-examination, computed tomography (CT) imaging, magnetic resonance imaging (MRI), positron emission tomography (PET), x-ray, ultrasound, biopsy, surgery, endoscopy, laparoscopy, and endoscopic retrograde cholangiopancreatography (ERCP). [0042]
  • In one embodiment, additional disease testing or follow-up analysis is used to determine where the disease resides. However, the general disease screen is effective independent of the location of the disease and the specimen taken for analysis. Thus, for example, while measurement of nucleic acid in stool is predictive of disease generally, it does not necessarily indicate that the disease is of gastrointestinal origin. However, follow-up testing or additional disease testing are used to identify the disease. [0043]
  • Methods of the invention may be practiced in accordance with protocols for diagnosing disease in a patient. In one embodiment, the quantitative amount of nucleic acid in a sample is measured as part of a protocol for diagnosing disease in a patient. FIGS. 1-5 describe particular examples of protocols for diagnosing disease in a patient. Although protocols in accordance with the invention are described with reference to specific embodiments, it should be understood by those skilled in the art that various changes in form and detail may be made therein without departing from the spirit and scope of the invention. [0044]
  • The flowchart in FIG. 1 describes a basic implementation of the present invention for diagnosing disease in a patient. At [0045] step 100, the quantitative amount of human DNA present in a the patient sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample. At step 102, if the amount of human DNA is lower than a predetermined threshold amount, then the patient is deemed healthy (or disease-free) in step 104. Also at step 102, if the amount of human DNA is higher than a predetermined threshold amount, then additional disease testing is performed on the patient in step 104. This additional disease testing can be any of those described herein or any other disease testing known in the art.
  • The flowchart in FIG. 2 describes a more detailed implementation of the present invention for diagnosing disease in a patient. At [0046] step 200, the amount of human DNA in a sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample. At step 202, if the amount of human DNA is lower than a predetermined threshold amount, then the patient is deemed healthy (or disease-free) in step 204. Also at step 102, if the amount of human DNA is higher than a predetermined threshold amount, then a DNA integrity test is performed on a sample from the patient in step 206. At step 208, if a positive screen is obtained from the DNA integrity test, then a colonoscopy is performed on the patient in step 210. Also at step 208, if a negative screen is obtained from the DNA integrity test, then the patient is deemed healthy (or disease-free) in step 204.
  • The flowchart in FIG. 3 describes a further detailed implementation of the present invention for diagnosing disease in a patient. At [0047] step 300, the amount of human DNA in a sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample. At step 302, if the amount of human DNA is lower than a predetermined threshold amount, then the patient is deemed healthy (or disease-free) in step 304. Also at step 302, if the amount of human DNA is higher than a predetermined threshold amount, then a DNA integrity test is performed on a sample from the patient in step 306. At step 308, if a positive result is obtained from the DNA integrity test, then a colonoscopy is performed on the patient in step 310. Also at step 308, if a negative result is obtained from the DNA integrity test, then a mutation detection assay is performed on a sample from the patient in step 312. At step 314, if a positive result is obtained from the mutation detection assay (i.e. a mutation is detected), then a colonoscopy is performed on the patient in step 310. Also at step 314, if a negative result is obtained from the mutation detection assay (i.e., a mutation is not detected), then the patient is deemed healthy (or disease-free) in step 316.
  • The flowchart in FIG. 4 describes an even further detailed implementation of the present invention for diagnosing disease in a patient. At [0048] step 400, the amount of human DNA in a sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample. At step 402, if the amount of human DNA is lower than a predetermined threshold amount, then a mutation detection assay is performed on the patient in step 404. At step 406, if a positive result is obtained from the mutation detection assay, then a colonoscopy is performed on the patient in step 408. Also at step 406, if a negative result is obtained from the mutation detection assay, then the patient is examined for symptoms of disease in step 410. If the patient is not symptomatic for disease, then the patient is deemed healthy (or disease-free) in step 426. If the patient is symptomatic for disease, then a DNA integrity assay is performed on a sample from the patient in step 412. At step 414, if a positive result is obtained from the DNA integrity test, then an upper gastrointestinal work-up is performed on the patient in step 416, followed by a colonoscopy in step 408. Also at step 414, if a negative result is obtained from the DNA integrity test, then the patient is deemed healthy (or disease-free) in step 426.
  • At [0049] step 402, if the amount of human DNA is higher than a predetermined threshold amount, then a DNA integrity test is performed on a sample from the patient in step 418. At step 420, if a positive result is obtained from the DNA integrity test, then a colonoscopy is performed on the patient in step 408. Also at step 420, if a negative result is obtained from the DNA integrity test, then a mutation detection assay is performed on a sample from the patient in step 422. At step 424, if a positive result is obtained from the mutation detection assay, then a colonoscopy is performed on the patient in step 408. Also at step 424, if a negative result is obtained from the mutation detection assay, then the patient is deemed healthy (or disease-free) in step 426.
  • The flowchart in FIG. 5 describes a detailed implementation of the present invention for diagnosing colorectal cancer in a patient. At [0050] step 500, the amount of human DNA in a sample is determined. In certain embodiments, the amount of human DNA is determined as a number of GEs in the sample. At step 502, if the amount of human DNA is lower than a predetermined threshold amount, then a mutation detection assay is performed on the patient in step 504. At step 506, if a positive result is obtained from the mutation detection assay, then a supracolonic work-up is performed on the patient in step 508. At step 506, if a negative result is obtained from the mutation detection assay, then the patient is deemed healthy in step 510.
  • At [0051] step 502, if the amount of human DNA is higher than a predetermined threshold amount, then a DNA integrity test is performed on a sample from the patient in step 512. At step 514, if a positive result is obtained from the DNA integrity test, then a colonoscopy is performed on the patient in step 516. Also at step 514, if a negative result is obtained from the DNA integrity test, then a mutation detection assay is performed on a sample from the patient in step 518. At step 520, if a positive result is obtained from the mutation detection assay, then a colonoscopy is performed on the patient in step 516. Also at step 520, if a negative result is obtained from the mutation detection assay, then the patient is deemed healthy in step 510.
  • The present invention provides relatively cost-effective screening methods that can be administered to a patient prior to performing additional disease testing. Methods of the invention are useful as general disease screening techniques, and are useful as screens for a wide-range of disease states. Methods of the inventions are also useful as screening techniques for the presence of cancer and pre-cancer, and are especially useful as screening techniques colorectal cancer and pre-cancer. In addition to colorectal cancers, methods of the invention are useful to screen for other cancers, for example, as screening techniques for lymphomas, stomach cancers, lung cancers, liver cancers, pancreas cancers, prostrate cancers, kidney cancers, testicular cancers bladder cancers, gallbladder cancers, uterine cancers, and ovarian cancers. Methods of the invention are also useful for screening for the presence of cancerous or precancerous lesions in a patient, including adenomas. [0052]
  • In addition to cancer, methods of the invention are useful, for example, as screening techniques for diseases such as inflammatory bowel syndrome, inflammatory bowel disease, Crohn's disease, respiratory distress syndrome, and others in which the performance of diagnostic procedures followed by the performance of screening methods of the invention would be effective in the detection of disease. Furthermore, the methods of the invention are also useful for detecting an indicator of the presence of an infectious agent, including, but not limited to, a virus, bacterium, parasite, or other microorganism. The invention is equally applicable to human and to veterinary uses. Accordingly, “patient” as discussed herein is intended to included humans and other animals. [0053]
  • In one embodiment, methods of the invention are used to monitor the progress of a disease in a patient or in populations of patients. Such longitudinal monitoring provides information on the degree to which the quantitative amount of nucleic acid in samples is increasing or decreasing as disease progresses or recedes. Longitudinal monitoring of the total genomic DNA in a patient sample can be done without reference to an external predetermined threshold and, instead, uses amounts determined at prior time point(s) as the predetermined threshold. For example, the nucleic acid in a patient's sample can be quantified at two or more time points. If the amount of nucleic acid increases from one or more previous time points, the patient can be tested with follow up additional disease testing. Alternatively, the amount of nucleic acid in a patient's sample can be quantified at two or more time points, and, if the amount of nucleic acid decreases from one or more previous time points and if the patient is being treated for a disease, the patient may show signs of partial or total abatement, alleviation, or treatment of a disease. Generally, such longitudinal monitoring can be used to assess the efficacy of treatments (e.g., chemotherapy, antibiotics), and the response of patients to therapeutic interventions. Methods of the invention can also be used to predict disease flare-up. For example, monitoring fluctuations in the quantitative amount of nucleic acids in samples from diseased patients, such as patients with inflammatory bowel disease, is useful to predict onset of disease episodes. According to the invention, episodic occurrence of symptoms is tied to an increase in the quantitative amount of nucleic acids in patient samples. [0054]
  • Methods of the invention are also useful to establish patient databases. Such databases are used to identify specific patients, to establish where a particular patient fits in a disease continuum, to follow trends in disease, to predict disease onset, or to compile statistics on disease frequency, to monitor patient progress and treatment efficacy, and the like. [0055]
  • Methods of the invention are also useful to predict risk for disease and to predict disease onset. Levels of nucleic acids in patient samples are useful as a quantitative or quasi-quantitative measure of disease. Thus, the level of, for example, nucleic acids obtained from a patient sample is compared to predetermined threshold amounts representing various stages of disease in order to assess the patient's disease state and prognosis. [0056]
  • The following examples provide further details of methods according to the invention. For purposes of exemplification, the following examples provide details of the use of methods of the present invention in colorectal cancer detection. Accordingly, while exemplified in the following manner, the invention is not so limited and the skilled artisan will appreciate its wide range of application upon consideration thereof. [0057]
  • EXAMPLE 1 Determination of Threshold Amount
  • In this example, methods of the invention were correlated with the clinical outcome in 49 patients who were previously diagnosed (using colonoscopy) as having colorectal cancer, and 100 patients who were diagnosed as not having colorectal cancer. The threshold amount (the amount at which patients below such amount can be identified as being relatively disease-free) for use in methods of the invention was empirically determined as described below. [0058]
  • Stool specimens were collected from patients and frozen. Each frozen stool specimen, weighing approximately 32 grams, was thawed and homogenized in buffer. The buffer was comprised of 0.5 M Tris, 10 mM NaCl, and 150 mM EDTA, essentially as disclosed in U.S. Pat. No. 6,551,777, incorporated by reference herein. Each of the samples was then diluted with additional buffer (not containing EDTA) to a final buffer to stool ratio of 20:1. Each sample was centrifuged, and the supernatant, which carried the active DNA degrading fraction, was removed to a clean tube. The supernatant was collected and treated with sodium dodecyl sulfate and Proteinase K. The DNA in each sample was then prepared by standard techniques. See, e.g., Ausubel et al., [0059] Short Protocols in Molecular Biology §§ 2.1-2.4 (3d ed. 1995). A phenol extraction, a phenol/chloroform extraction, and a phenol extraction were performed prior to isolating the DNA. The isolated DNA was then placed into a standard. Tris buffer.
  • The DNA samples were amplified using quantitative PCR. A PCR primer set from Midland Certified Reagent Company, TaqMan® probes from PanVera Corporation and a real-time PCR instrument were used (Biorad Corporations's iCycler iQ Real Time PCR Detection System). TaqMan® analysis was performed on an ABI 7700 thermalcycler (Applied Biosystems, Foster City, Calif.) using primers against a 200 base pair region of the APC gene. The 5′ primer was: 5′AGCCCCAGTGATCTTCCAGAT3′ (SEQ ID NO: 1). The ′3 primer was: 5′AGGTGGTGGAGGTGTTTTACTTCT3′ (SEQ ID NO: 2). A FAM/TAMRA probe was used to detect amplified PCR product: FAM-CCCTGGACAAACCATGCCACCAA-TAMRA (SEQ ID NO: 3). [0060]
  • Amplification reactions consisted of captured human stool DNA mixed with TaqMan® PCR Universal Master mix (Applied Biosystems, Foster City, Calif.), 1×PCR primers (5 μmol/L), and 1×TaqMan® probe (2 μmol/L) (Applied Biosystems, Foster City, Calif.). 5 mls of captured DNA were used in PCR reactions. TaqMan® reactions were performed as follows. Thermal cycling began with a primer annealing step (50° C. for 2 min) and one cycle of DNA denaturation (95° C. for 10 minutes). This was followed by 40 cycles of sequential DNA denaturation (95° C. for 1 min) and primer annealing (60° C. for 1 min). The ABI 7700 unit detected amplification products with the FAM/TAMRA probe and data used in the calculation of genome equivalents per reaction was provided. Clinical status was determined by performing a colonoscopy on each patient. The results are shown in the Table 1 below. [0061]
    TABLE 1
    Patient No. Clinical Status GE
    PV-11 Normal 147
    PV-64 Normal 155
    PV-109 Normal 163
    PV-10 Normal 168
    PV-27 Normal 180
    PV-56 Normal 266
    PV-119 Normal 272
    PV-59 Normal 312
    PV-137 Normal 334
    PV-8 Minor Polyps 386
    PV-52 Normal 394
    PV-96 Normal 404
    PV-44 Normal 490
    PV-3 Minor Polyps 498
    PV-57 Minor polyps 536
    PV-23 Normal 574
    PV-81 Minor Polyps 630
    PV-111 Dukes A 652
    PV-141 Normal 688
    PV-84 Normal 736
    PV-5 Normal 746
    PV-106 Normal 756
    PV-19 Dukes A 772
    PV-89 Normal 788
    PV-39 Dukes C 834
    PV-99 Minor Polyps 844
    PV-146 Minor Polyps 850
    PV-105 Minor Polyps 886
    PV-1 Minor Polyps 940
    PV-73 Normal 952
    PV-140 Normal 1,038
    PV-28 Dukes B 1,138
    PV-16 Normal 1,226
    PV-9 Normal 1,246
    PV-68 Dukes A 1,262
    PV-60 Dukes B 1,290
    PV-130 Minor Polyps 1,302
    PV-22 Minor Polyps 1,312
    PV-63 Normal 1,334
    PV-123 Minor Polyps 1,334
    PV-118 Minor Polyps 1,354
    PV-124 Normal 1,468
    PV-35 Minor Polyps 1,510
    PV-133 Normal 1,510
    PV-4 Minor Polyps 1,564
    PV-72 Normal 1,582
    PV-41 Normal 1,604
    PV-53 Dukes A 1,670
    PV-147 Minor Polyps 1,688
    PV-40 Dukes C 1,870
    PV-114 Minor Polyps 1,936
    PV-92 Minor Polyps 1,956
    PV-113 Minor Polyps 1,982
    PV-121 Normal 2,040
    PV-136 Minor Polyps 2,080
    PV-125 Minor Polyps 2,120
    PV-132 Normal 2,120
    PV-138 Normal 2,140
    PV-112 Minor Polyps 2,180
    PV-12 Dukes A 2,200
    PV-128 Minor Polyps 2,240
    PV-148 Minor Polyps 2,240
    PV-150 Normal 2,260
    PV-62 Normal 2,360
    PV-43 Minor Polyps 2,420
    PV-100 Minor Polyps 2,540
    PV-104 Minor Polyps 2,560
    PV-2 Minor Polyps 2,580
    PV-90 Minor Polyps 2,600
    PV-117 LCD 2,620
    PV-95 Minor Polyps 2,640
    PV-85 Normal 2,660
    PV-26 Normal 2,720
    PV-17 Normal 2,760
    PV-108 Minor Polyps 2,800
    PV-144 Normal 2,820
    PV-120 Minor Polyps 2,880
    PV-143 Minor Polyps 2,880
    PV-37 Minor Polyps 2,940
    PV-107 Minor Polyps 3,020
    PV-71 Dukes B 3,140
    PV-38 Dukes C 3,200
    PV-30 Normal 3,220
    PV-7 Dukes A 3,220
    PV-66 Normal 3,440
    PV-86 Dukes C 3,520
    PV-126 Normal 3,540
    PV-115 Minor Polyps 3,560
    PV-51 Normal 3 640
    PV-145 Normal 3,660
    PV-29 Dukes B 3,840
    PV-65 Dukes B 3,940
    PV-14 Minor Polyps 4,180
    PV-46 Dukes C 4,200
    PV-36 Dukes A 4,300
    PV-49 Minor Polyps 4,420
    PV-47 Dukes C 4,420
    PV-34 Dukes A 4,440
    PV-139 Minor Polyps 4,740
    PV-82 Normal 4,980
    PV-79 Minor Polyps 5,000
    PV-58 Dukes B 5,000
    PV-98 Dukes A 5,140
    PV-67 Dukes A 5,220
    PV-134 Normal 5,240
    PV-33 Dukes D 5,240
    PV-31 CIS/HGD 5,500
    PV-122 Normal 5,560
    PV-129 Normal 5,560
    PV-45 Minor Polyps 5,620
    PV-97 Minor Polyps 5,940
    PV-149 Normal 6,080
    PV-116 Normal 6,120
    PV-74 Normal 6,180
    PV-102 Dukes A 6,980
    PV-83 Normal 7,160
    PV-93 Dukes C 7,860
    PV-131 Minor Polyps 7,900
    PV-61 Dukes B 7,940
    PV-127 Minor Polyps 8,020
    PV-55 Dukes C 8,240
    PV-69 Dukes B 8,280
    PV-76 Dukes D 9,460
    PV-25 Minor Polyps 9,580
    PV-94 Minor Polyps 9,780
    PV-15 Dukes A 10,500
    PV-135 Minor Polyps 10,580
    PV-110 Minor Polyps 11,620
    PV-20 Dukes B 11,960
    PV-142 Normal 13,240
    PV-54 Dukes C 14,620
    PV-70 Dukes C 15,620
    PV-21 Dukes B 17,940
    PV-87 Dukes C 18,180
    PV-32 Dukes C 20,400
    PV-91 Normal 22,400
    PV-78 Normal 23,000
    PV-6 Dukes A 25,400
    PV-77 Dukes C 25,600
    PV-42 Dukes C 27,600
    PV-50 Normal 28,000
    PV-24 Dukes B 29,200
    PV-88 Dukes C 32,800
    PV-80 Dukes A 54,600
    PV-101 Dukes B 59,600
    PV-75 Dukes C 90,400
    PV-13 Dukes A 138,600
    PV-103 Dukes C 141,800
    PV-18 Dukes A 238,000
    PV-48 CIS 286,000
  • In reference to the table above, the diagnoses of “normal” or “minor polyps” are considered “normal patients” as discussed herein. Also, the diagnoses of “Dukes A,” “Dukes B,” “Dukes C” (refers to the stages of colorectal cancer), “LGD” (Low Grade Dysplasia), “HGD” (High Grade Dysplasia), and “CIS” (Carcinoma In Situ) are considered “cancer patients” as discussed herein. [0062]
  • As shown in the table above, there is overlap of GE scores for normal patients and cancer patients. The lowest GE score for a cancer patient was 652 and the lowest GE score for a normal patient was 147. However, there were 17 normal patients with GE scores lower than the lowest GE score for a cancer patient (652). Accordingly, using this data set, the predetermined threshold amount for use in methods of the invention can be set to any score below 652. As one example, the GE score can be set at 650. Based on this score, 17% of normal patients would not have to undergo additional disease testing. As another example, the GE score can be set at 630 (i.e., the highest number of GEs for a normal patient that is less than the lowest number of GEs for a cancer patient). Based on this score, 16% of normal patients would not have to undergo additional disease testing. As further example, the GE score can be set at 500 to eliminate potential false-negatives in future testing. Based on this score, 14% of normal patients would not have to undergo additional disease testing. As another example, the GE score can be set at 250. Based on this score, 9% of normal patients would not have to undergo additional disease testing. As a further example, the GE score can be set at 200. Based on this score, 5% of normal patients would not have to undergo additional disease testing. As a further example, the GE score can be set at 700 to eliminate potential false-positives in future testing. [0063]
  • Using methods of the invention, a subset of the patient population would not have to undergo additional disease testing based on GE scores below the predetermined threshold amount. To reduce the likelihood of false-negative results using methods of the invention, the same preparation methods, amplification methods, and quantitative analysis methods that were used to determined the threshold amount should be used when screening patient samples in accordance with the invention. [0064]
  • EXAMPLE 2
  • According to methods of the invention, if the amount of DNA in a patient sample is greater than the predetermined threshold amount, then the patient is identified as a candidate for additional disease testing. For example, if the predetermined threshold amount is 1,000 GEs, and a patient sample measures 50,000 GEs, then the patient would be a candidate for additional disease testing. Example 3 describes another preferred method of additional disease testing in accordance with the invention. [0065]
  • Additional Disease Testing: DNA Integrity Assay
  • Detection of DNA fragments of at least 200 base pairs in length are also useful in an additional disease testing phase of the invention, as the amount of 200 bp or greater DNA in a sample is predictive of cancer or precancer in patients. The samples are screened by hybrid capturing human DNA and determining the amount of amplifiable DNA having at least 200 base pairs. Stool samples are prepared as described in Example 1. [0066]
  • Human DNA is isolated from stool precipitate by sequence-specific hybrid capture. Biotynilated probes against portions of the p53, K-ras, and ape genes are used. The K-ras probe is 5′GTGGAGTATTTGATAGTGTATTAACCTTATGTGTGAC 3′ (SEQ ID NO: 4). There are two apc probes. The apc-1309 probe is 5′TTCCAGCAGTGTCACAGCACCCTAGAACCAAATCCAG 3′ (SEQ ID NO: 5), and the apc-1378 probe is 5′CAGATAGCCCTGGACAAACAATGCCACGAAGCAGAAG 3′ (SEQ ID NO: 6). There are four probes against p53. The first (hybridizing to a portion of exon 5) is 5′TACTCCCCTGCCCTCAACAAGATGTTTTGCCAACTGG3′ (SEQ ID NO: 7), the second (hybridizing to a portion of exon 7) is 5′ATTTCTTCCATACTACTACCCATCGACCTCTCATC3′ (SEQ ID NO: 8), the third, also hybridizing to a portion of exon 7 is 5′ATGAGGCCAGTGCGCCTTGGGGAGACCTGTGGCAAGC3′ (SEQ ID NO: 9); and finally, a probe against exon 8 has the sequence 5′GAAAGGACAAGGGTGGTTGGGAGTAGATGGAGCCTGG3′ (SEQ ID NO: 10). A 10 μl aliquot of each probe (20 pmol/capture) is added to a suspension containing 300 μl DNA in the presence of 310 μl 6M GITC buffer for 2 hours at room temperature. Hybrid complexes are isolated using streptavidin-coated beads (Dynal). After washing, probe-bead complexes are suspended at 25° C. for 1 hour in 0.1×TE buffer, pH7.4. The suspension is then heated for 4 minutes at 85° C., and the beads are removed. [0067]
  • Each sample is amplified using forward and reverse primers through 7 loci (Kras, exon 1, APC exon 15 (3 separate loci), p53, exon 5, p53, exon 7, and p53, exon 8) in duplicate (for a total of 14 amplifications for each locus). Seven separate PCRs (33 cycles each) are run in duplicate using primers directed to detect fragments in the sample having 200 base pairs or more. Amplified DNA is placed on a 4% Nusieve (FMC Biochemical) gel (3% Nusieve, 1% agarose), and stained with ethidium bromide (0.5 μg/ml). The resulting amplified DNA is graded based upon the relative intensity of the stained gels. Samples from a patient with cancer or adenoma are detected as a band having significantly greater intensity than the bands associated with samples from patients who do not have cancer or precancer. Patients are identified as having cancer or adenoma by determining the amount of amplifiable DNA measuring 200 base pairs or greater in length. [0068]
  • EXAMPLE 3
  • According to methods of the invention, if the amount of DNA in a patient sample is greater than the predetermined threshold amount, then the patient is identified as a candidate for additional disease testing. For example, if the predetermined threshold amount is 500 GEs, and a patient sample measures 20,000 GEs, then the patient would be a candidate for additional disease testing. Example 2 describes a preferred method of additional disease testing in accordance with the invention. [0069]
  • Additional Disease Testing: Detection of BAT-26 Mutation
  • The BAT-26 segment of the MSH1 mismatch repair locus (shown in SEQ ID NO: 11) is useful in the additional disease testing phase of the invention, as-deletions in BAT-26 have been associated with colorectal cancer. Stool samples are prepared as described in Example 1. [0070]
  • A primer is hybridized to the portion of the BAT-26 locus immediately upstream of the poly-A tract, which consists of 26 adenosines (nucleotides 195-221). Unlabeled deoxythymidine, a mixture of labeled and unlabeled deoxycytosine, and unlabeled dideoxyadenine are added along with polymerase. The primer is extended through the poly-A region. The labeled and unlabelled cytosine is extended for the next three bases (nucleotides 222-224, all guanines in the intact sequence) such that label is incorporated into each extended primer. After the poly-A tract and the three guanines, there exist two thymidines in the intact sequence. Thus, the dideoxyadenosine stops primer extension by addition at the end of a primer that is extended through the poly-A and triguanine regions. Strands are separated, and the length of the strands are observed on a polyacrylamide gel to detect deletions in the poly-A tract. Deletions in the poly-A tract are indicative of colorectal cancer. [0071]
  • Although details of the present invention have been described with reference to specific and preferred embodiments, it should be understood by those skilled in the art that various changes in form and detail may be made therein without departing from the spirit and scope of the invention. [0072]
  • 1 11 1 21 DNA Artificial Sequence Primer 1 agccccagtg atcttccaga t 21 2 24 DNA Artificial Sequence Primer 2 aggtggtgga ggtgttttac ttct 24 3 23 DNA Artificial Sequence Probe 3 ccctggacaa accatgccac caa 23 4 37 DNA Artificial Sequence Probe 4 gtggagtatt tgatagtgta ttaaccttat gtgtgac 37 5 37 DNA Artificial Sequence Probe 5 ttccagcagt gtcacagcac cctagaacca aatccag 37 6 37 DNA Artificial Sequence Probe 6 cagatagccc tggacaaaca atgccacgaa gcagaag 37 7 37 DNA Artificial Sequence Probe 7 tactcccctg ccctcaacaa gatgttttgc caactgg 37 8 35 DNA Artificial Sequence Probe 8 atttcttcca tactactacc catcgacctc tcatc 35 9 37 DNA Artificial Sequence Probe 9 atgaggccag tgcgccttgg ggagacctgt ggcaagc 37 10 37 DNA Artificial Sequence Probe 10 gaaaggacaa gggtggttgg gagtagatgg agcctgg 37 11 314 DNA Homo Sapiens misc_feature (246)..(253) n corresponds to a nucleotide of unknown identity. 11 ccagtggtat agaaatcttc gatttttaaa ttcttaattt taggttgcag tttcatcact 60 gtctgcggta atcaagtttt tagaactctt atcagatgat tccaactttg gacagtttga 120 actgactact tttgacttca gccagtatat gaaattggat attgcagcag tcagagccct 180 taaccttttt caggtaaaaa aaaaaaaaaa aaaaaaaaaa agggttaaaa atgttgattg 240 gttaannnnn nnngacagat agtgaagaag gcttagaaag gagctaaaag agttcgacat 300 caatattaga caag 314

Claims (32)

What is claimed is:
1. A method for screening a patient for the presence of disease, comprising the steps of:
measuring a quantitative amount of nucleic acid in a patient sample comprising shed cells or cellular debris; and
identifying the patient as a candidate for additional disease testing if the amount of nucleic acid is above a predetermined threshold amount.
2. The method of claim 1, wherein the nucleic acid is genomic DNA.
3. The method of claim 1, wherein the measuring comprises determining a number of genome equivalents.
4. The method of claim 1, further comprising the step of performing an assay on a sample from the patient if the patient is identified as a candidate for additional disease testing.
5. The method of claim 4, wherein the assay is selected from the group consisting of a DNA integrity assay, mutation detection, enumerated LOH, expression assays, and FISH.
6. The method of claim 4, wherein the assay detects mutations at a genetic locus selected from the group consisting of p53, ras, APC, DCC, and BAT-26.
7. The method of claim 1, further comprising the step of performing a diagnostic examination on the patient if the patient is identified as a candidate for additional disease testing.
8. The method of claim 7, wherein the step of performing a diagnostic examination is selected from a group consisting of a colonoscopy, a sigmoidoscopy, a fecal occult blood testing and an upper gastrointestinal evaluation.
9. The method of claim 1, wherein the patient sample is stool.
10. The method of claim 1, wherein the patient sample is selected from the group consisting of sputum, pancreatic fluid, bile, lymph, blood, urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and pus.
11. The method of claim 1, wherein the disease is cancer or pre-cancer.
12. The method of claim 11, wherein the cancer is colorectal cancer.
13. The method of claim 11, wherein the cancer is selected from the group consisting of lung cancer, esophageal cancer, prostrate cancer, stomach cancer, pancreatic cancer, liver cancer, and lymphoma.
14. A method for screening a patient for the presence of abnormal proliferating cells, comprising the steps of:
measuring a quantitative amount of nucleic acid in a patient sample comprising shed cells or cellular debris; and
identifying a positive screen as a sample in which the amount of nucleic acid is above a predetermined threshold amount.
15. The method of claim 14, wherein the nucleic acid is genomic DNA.
16. The method of claim 14, wherein the measuring comprises determining a number of genome equivalents.
17. The method of claim 14, further comprising the step of performing an assay on a sample from the patient if a positive screen is identified in the identifying step.
18. The method of claim 17, wherein the assay is selected from the group consisting of a DNA integrity assay, mutation detection, enumerated LOH, expression assays, and FISH.
19. The method of claim 17, wherein the assay detects mutations at a genetic locus selected from the group consisting of p53, ras, APC, DCC, and BAT-26.
20. The method of claim 14, further comprising the step of performing a diagnostic examination on the patient if a positive screen is identified in the identifying step.
21. The method of claim 20, wherein the step of performing a diagnostic examination is selected from a group consisting of a colonoscopy, a sigmoidoscopy, a fecal occult blood testing and an upper gastrointestinal evaluation.
22. The method of claim 14, wherein the patient sample is stool.
23. The method of claim 14, wherein the patient sample is selected from the group consisting of sputum, pancreatic fluid, bile, lymph, blood, urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and pus.
24. A method for diagnosing the state of health of a patient, comprising the steps of:
measuring a quantitative amount of nucleic acid in a patient sample comprising shed cells or cellular debris; and
performing an assay on a sample from the patient if the amount of nucleic acid is above a predetermined threshold amount, wherein the state of health of a patient is determined.
25. The method of claim 24, wherein the nucleic acid is genomic DNA.
26. The method of claim 24, wherein the measuring comprises determining a number of genome equivalents.
27. The method of claim 24, wherein the assay is selected from the group consisting of a DNA integrity assay, mutation detection, enumerated LOH, expression assays, and FISH.
28. The method of claim 24, wherein the assay detects mutations at a genetic locus selected from the group consisting of p53, ras, APC, DCC, and BAT-26.
29. The method of claim 24, wherein the method further comprises performing a diagnostic examination on the patient.
30. The method of claim 29, wherein the diagnostic examination is selected from a group consisting of a colonoscopy, a sigmoidoscopy, a fecal occult blood testing and an upper gastrointestinal evaluation.
31. The method of claim 24, wherein the patient sample is stool.
32. The method of claim 24, wherein the patient sample is selected from the group consisting of sputum, pancreatic fluid, bile, lymph, blood, urine, cerebrospinal fluid, seminal fluid, saliva, breast nipple aspirate, and pus.
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050014165A1 (en) * 2003-07-18 2005-01-20 California Pacific Medical Center Biomarker panel for colorectal cancer
WO2009104714A1 (en) * 2008-02-22 2009-08-27 株式会社ジーンサイエンス Early genetic test method for cancer
US20100124743A1 (en) * 2007-01-23 2010-05-20 Olympus Corporation Method for diagnosis of cancer
US20100255481A1 (en) * 2007-10-30 2010-10-07 Olympus Corporation Method for detection of adenoma or cancer by genetic analysis
US20100261221A1 (en) * 2007-07-26 2010-10-14 California Pacific Medical Center Method to predict or diagnose a gastrointestinal disorder or disease
WO2014181816A1 (en) 2013-05-08 2014-11-13 有限会社マイテック Raman quantification method of cancer-related substance
WO2016120475A1 (en) * 2015-01-30 2016-08-04 Enterome Host dna as a biomarker of crohn's disease
US10400283B2 (en) 2007-05-31 2019-09-03 Nancy M. Lee Method to predict or diagnose a gastrointestinal disorder or disease
USRE49542E1 (en) * 2005-04-06 2023-06-06 Guardant Health, Inc. Method for the detection of cancer

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9109256B2 (en) * 2004-10-27 2015-08-18 Esoterix Genetic Laboratories, Llc Method for monitoring disease progression or recurrence
US9777314B2 (en) 2005-04-21 2017-10-03 Esoterix Genetic Laboratories, Llc Analysis of heterogeneous nucleic acid samples

Citations (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4101279A (en) * 1977-04-06 1978-07-18 Muhammed Javed Aslam Device for the collection and processing of stool specimens
US4309782A (en) * 1980-09-11 1982-01-12 Esteban Paulin Device for collecting fecal specimens
US4333734A (en) * 1980-01-18 1982-06-08 Sloan-Kettering Institute For Cancer Research Diagnostic device for fecal occult blood and method of use
US4445235A (en) * 1982-09-13 1984-05-01 Pearl Slover Stool specimen collector
US4535058A (en) * 1982-10-01 1985-08-13 Massachusetts Institute Of Technology Characterization of oncogenes and assays based thereon
US4578358A (en) * 1983-05-03 1986-03-25 Warner-Lambert Company Collection of specimens and detection of occult blood therein
US4735905A (en) * 1986-08-15 1988-04-05 V-Tech, Inc. Specimen-gathering apparatus and method
US4857300A (en) * 1987-07-27 1989-08-15 Cytocorp, Inc. Cytological and histological fixative formulation and methods for using same
US4935342A (en) * 1986-12-01 1990-06-19 Syngene, Inc. Method of isolating and purifying nucleic acids from biological samples
US4981783A (en) * 1986-04-16 1991-01-01 Montefiore Medical Center Method for detecting pathological conditions
US4982615A (en) * 1988-04-18 1991-01-08 Bernard Sultan Sterile container for collecting biological samples for purposes of analysis
US5087617A (en) * 1989-02-15 1992-02-11 Board Of Regents, The University Of Texas System Methods and compositions for treatment of cancer using oligonucleotides
US5126239A (en) * 1990-03-14 1992-06-30 E. I. Du Pont De Nemours And Company Process for detecting polymorphisms on the basis of nucleotide differences
US5137806A (en) * 1989-12-11 1992-08-11 Board Of Regents, The University Of Texas System Methods and compositions for the detection of sequences in selected DNA molecules
US5196167A (en) * 1989-04-04 1993-03-23 Helena Laboratories Corporation Fecal occult blood test product with positive and negative controls
US5200314A (en) * 1990-03-23 1993-04-06 Chiron Corporation Polynucleotide capture assay employing in vitro amplification
US5248671A (en) * 1989-02-15 1993-09-28 Board Of Regents, The University Of Texas System Methods and compositions for treatment of cancer using oligonucleotides
US5302509A (en) * 1989-08-14 1994-04-12 Beckman Instruments, Inc. Method for sequencing polynucleotides
US5330892A (en) * 1991-03-13 1994-07-19 The Johns Hopkins University MCC gene (mutated in colorectal cancer) used for diagnosis of cancer in humans
US5331973A (en) * 1993-03-15 1994-07-26 Fiedler Paul N Method for obtaining stool samples for gastrointestinal cancer testing
US5348855A (en) * 1986-03-05 1994-09-20 Miles Inc. Assay for nucleic acid sequences in an unpurified sample
US5378602A (en) * 1991-05-29 1995-01-03 The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Highly informative microsatellite repeat polymorphic DNA markers twenty-[seven]six
US5380645A (en) * 1989-03-16 1995-01-10 The Johns Hopkins University Generalized method for assessment of colorectal carcinoma
US5380647A (en) * 1991-02-05 1995-01-10 Farrokh Saidi Simple test for detecting carcinoembryonic antigen in stool
US5382510A (en) * 1990-06-27 1995-01-17 The Trustees Of Princeton University Methods of diagnosing pre-cancer or cancer states using probes for detecting mutant p53
US5409586A (en) * 1992-08-26 1995-04-25 Hitachi, Ltd. Method for analyzing nucleic acid or protein and apparatus therefor
US5416025A (en) * 1993-11-29 1995-05-16 Krepinsky; Jiri J. Screening test for early detection of colorectal cancer
US5482834A (en) * 1982-05-17 1996-01-09 Hahnemann University Evaluation of nucleic acids in a biological sample hybridization in a solution of chaotrophic salt solubilized cells
US5489508A (en) * 1992-05-13 1996-02-06 University Of Texas System Board Of Regents Therapy and diagnosis of conditions related to telomere length and/or telomerase activity
US5492808A (en) * 1993-05-05 1996-02-20 The Johns Hopkins University Means for detecting familial colon cancer (FCC)
US5496470A (en) * 1994-05-27 1996-03-05 Barnes International, Inc. Magnetic separator
US5506105A (en) * 1991-12-10 1996-04-09 Dade International Inc. In situ assay of amplified intracellular mRNA targets
US5508164A (en) * 1990-10-29 1996-04-16 Dekalb Genetics Corporation Isolation of biological materials using magnetic particles
US5512441A (en) * 1994-11-15 1996-04-30 American Health Foundation Quantative method for early detection of mutant alleles and diagnostic kits for carrying out the method
US5514547A (en) * 1991-02-05 1996-05-07 Lifecodes Corporation Molecular genetic identification using probes that recognize polymorphic loci
US5527676A (en) * 1989-03-29 1996-06-18 The Johns Hopkins University Detection of loss of the wild-type P53 gene and kits therefor
US5532108A (en) * 1990-01-04 1996-07-02 The Johns Hopkins University Gene deleted in colorectal cancer of humans
US5538851A (en) * 1993-12-22 1996-07-23 Institut Pasteur And Cneva Primers for the amplification of genes coding for the enterotoxin and the lecithinase of Clostridium perfringens and their application to the determination of the presence and numeration of these bacteriae
US5559014A (en) * 1989-11-08 1996-09-24 Baylor College Of Medicine Methods and reagents to detect and characterize Norwalk and related viruses
US5599662A (en) * 1995-02-17 1997-02-04 Hoffmann-La Roche Inc. Oliconucleotide primers and probes for the detection of HIV-1
US5612473A (en) * 1996-01-16 1997-03-18 Gull Laboratories Methods, kits and solutions for preparing sample material for nucleic acid amplification
US5635352A (en) * 1993-12-08 1997-06-03 Chiron Corporation Solution phase nucleic acid sandwich assays having reduced background noise
US5641628A (en) * 1989-11-13 1997-06-24 Children's Medical Center Corporation Non-invasive method for isolation and detection of fetal DNA
US5645995A (en) * 1996-04-12 1997-07-08 Baylor College Of Medicine Methods for diagnosing an increased risk for breast or ovarian cancer
US5670325A (en) * 1996-08-14 1997-09-23 Exact Laboratories, Inc. Method for the detection of clonal populations of transformed cells in a genomically heterogeneous cellular sample
US5710028A (en) * 1992-07-02 1998-01-20 Eyal; Nurit Method of quick screening and identification of specific DNA sequences by single nucleotide primer extension and kits therefor
US5709998A (en) * 1993-12-15 1998-01-20 The Johns Hopkins University Molecular diagnosis of familial adenomatous polyposis
US5741650A (en) * 1996-01-30 1998-04-21 Exact Laboratories, Inc. Methods for detecting colon cancer from stool samples
US5759777A (en) * 1989-04-05 1998-06-02 Amoco Corporation Hybridization promotion reagents
US5856104A (en) * 1996-10-28 1999-01-05 Affymetrix, Inc. Polymorphisms in the glucose-6 phosphate dehydrogenase locus
US5882865A (en) * 1996-03-22 1999-03-16 The Johns Hopkins University Cancer drug screen based on cell cycle uncoupling
US5888778A (en) * 1997-06-16 1999-03-30 Exact Laboratories, Inc. High-throughput screening method for identification of genetic mutations or disease-causing microorganisms using segmented primers
US5910407A (en) * 1992-04-01 1999-06-08 The Johns Hopkins University School Of Medicine Method for detection of target nucleic acid by analysis of stool
US5916744A (en) * 1993-03-22 1999-06-29 National Research Council Of Canada Testing for infestation of rapeseed and other cruciferae by the fungus Leptosphaeria maculans (blackleg infestation)
US5928870A (en) * 1997-06-16 1999-07-27 Exact Laboratories, Inc. Methods for the detection of loss of heterozygosity
US5942396A (en) * 1997-08-19 1999-08-24 The Rockefeller University Method for identifying individuals at risk for colorectal neoplasia by quantifying normal colonic mucosal epithelial cell apoptosis
US5952178A (en) * 1996-08-14 1999-09-14 Exact Laboratories Methods for disease diagnosis from stool samples
US6020137A (en) * 1996-08-14 2000-02-01 Exact Laboratories, Inc. Methods for the detection of loss of heterozygosity
US6037465A (en) * 1994-06-14 2000-03-14 Invitek Gmbh Universal process for isolating and purifying nucleic acids from extremely small amounts of highly contaminated various starting materials
US6084091A (en) * 1995-08-16 2000-07-04 Max-Planck-Gesellschaft Zur Forerung Der Wissenschaften E.V. Process for purifying, stabilising or isolating nucleic acids from biological materials
US6100029A (en) * 1996-08-14 2000-08-08 Exact Laboratories, Inc. Methods for the detection of chromosomal aberrations
US6203993B1 (en) * 1996-08-14 2001-03-20 Exact Science Corp. Methods for the detection of nucleic acids
US6214187B1 (en) * 1998-06-18 2001-04-10 Mosaic Technologies Denaturing gradient affinity electrophoresis and methods of use thereof
US6228596B1 (en) * 1998-03-05 2001-05-08 Diadexus, Inc. Method of detecting and monitoring endometrial and uterine cancers
US6235474B1 (en) * 1996-12-30 2001-05-22 The Johns Hopkins University Methods and kits for diagnosing and determination of the predisposition for diseases
US6238927B1 (en) * 1998-10-05 2001-05-29 Mosaic Technologies, Incorporated Reverse displacement assay for detection of nucleic acid sequences
US6251660B1 (en) * 1997-11-25 2001-06-26 Mosaic Technologies, Inc. Devices and methods for detecting target molecules in biological samples
US6268136B1 (en) * 1997-06-16 2001-07-31 Exact Science Corporation Methods for stool sample preparation
US6280947B1 (en) * 1999-08-11 2001-08-28 Exact Sciences Corporation Methods for detecting nucleotide insertion or deletion using primer extension
US20010018180A1 (en) * 1999-01-10 2001-08-30 Shuber Anthony P. Methods for detecting mutations using primer extension for detecting disease
US20020001800A1 (en) * 1998-08-14 2002-01-03 Stanley N. Lapidus Diagnostic methods using serial testing of polymorphic loci
US20020004201A1 (en) * 1997-06-16 2002-01-10 Lapidus Stanley N. Methods for the detection of loss of heterozygosity
US20020019472A1 (en) * 2000-06-13 2002-02-14 Fumio Yamashita Copolymer excelling in pigment dispersibility
US20020025525A1 (en) * 1997-10-23 2002-02-28 Shuber Anthony P. Methods for detecting contamination in molecular diagnostics using PCR
US6351857B2 (en) * 1999-05-03 2002-03-05 Exact Sciences Corporation Stool specimen collector
US20020048752A1 (en) * 1998-11-23 2002-04-25 Stanley N. Lapidus Methods for detecting lower-frequency molecules
US6406857B1 (en) * 1997-06-16 2002-06-18 Exact Sciences Corporation Methods for stool sample preparation
US6428964B1 (en) * 2001-03-15 2002-08-06 Exact Sciences Corporation Method for alteration detection
US20020110810A1 (en) * 2001-01-05 2002-08-15 Shuber Anthony P. Methods for detecting, grading or monitoring an H. pylori infection
US20020119469A1 (en) * 1996-08-14 2002-08-29 Shuber Anthony P. Methods for the detection of nucleic acids
US6448002B1 (en) * 1996-08-26 2002-09-10 Invitek Gmbh Method to detect clinically relevant mutations of the DNA sequence of ki-ras oncogene, its use and a testkit for early diagnosis of tumors
US20030044780A1 (en) * 1998-11-23 2003-03-06 Stanley N. Lapidus Primer extension methods utilizing donor and acceptor molecules for detecting nucleic acids
US20030049659A1 (en) * 2001-05-29 2003-03-13 Lapidus Stanley N. Devices and methods for isolating samples into subsamples for analysis
US6551777B1 (en) * 1999-02-25 2003-04-22 Exact Sciences Corporation Methods for preserving DNA integrity
US20030087258A1 (en) * 1997-10-23 2003-05-08 Shuber Anthony P. Methods for detecting hypermethylated nucleic acid in heterogeneous biological samples
US6586177B1 (en) * 1999-09-08 2003-07-01 Exact Sciences Corporation Methods for disease detection
US20040043467A1 (en) * 1999-12-07 2004-03-04 Shuber Anthony P. Supracolonic aerodigestive neoplasm detection
US6849403B1 (en) * 1999-09-08 2005-02-01 Exact Sciences Corporation Apparatus and method for drug screening
US6919174B1 (en) * 1999-12-07 2005-07-19 Exact Sciences Corporation Methods for disease detection

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020004206A1 (en) * 1999-04-09 2002-01-10 Berger Barry M. Methods of screening for disease
ITMI20030434A1 (en) * 2003-03-07 2004-09-08 Istituto Oncologico Romagnolo Coope Rativa Sociale METHOD FOR THE DETECTION OF COLON-RECTUM TUMORS.

Patent Citations (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4101279A (en) * 1977-04-06 1978-07-18 Muhammed Javed Aslam Device for the collection and processing of stool specimens
US4333734A (en) * 1980-01-18 1982-06-08 Sloan-Kettering Institute For Cancer Research Diagnostic device for fecal occult blood and method of use
US4309782A (en) * 1980-09-11 1982-01-12 Esteban Paulin Device for collecting fecal specimens
US5482834A (en) * 1982-05-17 1996-01-09 Hahnemann University Evaluation of nucleic acids in a biological sample hybridization in a solution of chaotrophic salt solubilized cells
US4445235A (en) * 1982-09-13 1984-05-01 Pearl Slover Stool specimen collector
US4535058A (en) * 1982-10-01 1985-08-13 Massachusetts Institute Of Technology Characterization of oncogenes and assays based thereon
US4578358A (en) * 1983-05-03 1986-03-25 Warner-Lambert Company Collection of specimens and detection of occult blood therein
US5348855A (en) * 1986-03-05 1994-09-20 Miles Inc. Assay for nucleic acid sequences in an unpurified sample
US4981783A (en) * 1986-04-16 1991-01-01 Montefiore Medical Center Method for detecting pathological conditions
US4735905A (en) * 1986-08-15 1988-04-05 V-Tech, Inc. Specimen-gathering apparatus and method
US4935342A (en) * 1986-12-01 1990-06-19 Syngene, Inc. Method of isolating and purifying nucleic acids from biological samples
US4857300A (en) * 1987-07-27 1989-08-15 Cytocorp, Inc. Cytological and histological fixative formulation and methods for using same
US4982615A (en) * 1988-04-18 1991-01-08 Bernard Sultan Sterile container for collecting biological samples for purposes of analysis
US5087617A (en) * 1989-02-15 1992-02-11 Board Of Regents, The University Of Texas System Methods and compositions for treatment of cancer using oligonucleotides
US5248671A (en) * 1989-02-15 1993-09-28 Board Of Regents, The University Of Texas System Methods and compositions for treatment of cancer using oligonucleotides
US5380645A (en) * 1989-03-16 1995-01-10 The Johns Hopkins University Generalized method for assessment of colorectal carcinoma
US5527676A (en) * 1989-03-29 1996-06-18 The Johns Hopkins University Detection of loss of the wild-type P53 gene and kits therefor
US5196167A (en) * 1989-04-04 1993-03-23 Helena Laboratories Corporation Fecal occult blood test product with positive and negative controls
US5759777A (en) * 1989-04-05 1998-06-02 Amoco Corporation Hybridization promotion reagents
US5302509A (en) * 1989-08-14 1994-04-12 Beckman Instruments, Inc. Method for sequencing polynucleotides
US5559014A (en) * 1989-11-08 1996-09-24 Baylor College Of Medicine Methods and reagents to detect and characterize Norwalk and related viruses
US5641628A (en) * 1989-11-13 1997-06-24 Children's Medical Center Corporation Non-invasive method for isolation and detection of fetal DNA
US5137806A (en) * 1989-12-11 1992-08-11 Board Of Regents, The University Of Texas System Methods and compositions for the detection of sequences in selected DNA molecules
US5532108A (en) * 1990-01-04 1996-07-02 The Johns Hopkins University Gene deleted in colorectal cancer of humans
US5126239A (en) * 1990-03-14 1992-06-30 E. I. Du Pont De Nemours And Company Process for detecting polymorphisms on the basis of nucleotide differences
US5200314A (en) * 1990-03-23 1993-04-06 Chiron Corporation Polynucleotide capture assay employing in vitro amplification
US5382510A (en) * 1990-06-27 1995-01-17 The Trustees Of Princeton University Methods of diagnosing pre-cancer or cancer states using probes for detecting mutant p53
US5508164A (en) * 1990-10-29 1996-04-16 Dekalb Genetics Corporation Isolation of biological materials using magnetic particles
US5514547A (en) * 1991-02-05 1996-05-07 Lifecodes Corporation Molecular genetic identification using probes that recognize polymorphic loci
US5380647A (en) * 1991-02-05 1995-01-10 Farrokh Saidi Simple test for detecting carcinoembryonic antigen in stool
US5330892A (en) * 1991-03-13 1994-07-19 The Johns Hopkins University MCC gene (mutated in colorectal cancer) used for diagnosis of cancer in humans
US5378602A (en) * 1991-05-29 1995-01-03 The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Highly informative microsatellite repeat polymorphic DNA markers twenty-[seven]six
US5506105A (en) * 1991-12-10 1996-04-09 Dade International Inc. In situ assay of amplified intracellular mRNA targets
US5910407A (en) * 1992-04-01 1999-06-08 The Johns Hopkins University School Of Medicine Method for detection of target nucleic acid by analysis of stool
US6177251B1 (en) * 1992-04-01 2001-01-23 The Johns Hopkins University Method for detection of target nucleic acid by analysis of stool
US5489508A (en) * 1992-05-13 1996-02-06 University Of Texas System Board Of Regents Therapy and diagnosis of conditions related to telomere length and/or telomerase activity
US5710028A (en) * 1992-07-02 1998-01-20 Eyal; Nurit Method of quick screening and identification of specific DNA sequences by single nucleotide primer extension and kits therefor
US5409586A (en) * 1992-08-26 1995-04-25 Hitachi, Ltd. Method for analyzing nucleic acid or protein and apparatus therefor
US5331973A (en) * 1993-03-15 1994-07-26 Fiedler Paul N Method for obtaining stool samples for gastrointestinal cancer testing
US5916744A (en) * 1993-03-22 1999-06-29 National Research Council Of Canada Testing for infestation of rapeseed and other cruciferae by the fungus Leptosphaeria maculans (blackleg infestation)
US5492808A (en) * 1993-05-05 1996-02-20 The Johns Hopkins University Means for detecting familial colon cancer (FCC)
US5416025A (en) * 1993-11-29 1995-05-16 Krepinsky; Jiri J. Screening test for early detection of colorectal cancer
US5635352A (en) * 1993-12-08 1997-06-03 Chiron Corporation Solution phase nucleic acid sandwich assays having reduced background noise
US5709998A (en) * 1993-12-15 1998-01-20 The Johns Hopkins University Molecular diagnosis of familial adenomatous polyposis
US5538851A (en) * 1993-12-22 1996-07-23 Institut Pasteur And Cneva Primers for the amplification of genes coding for the enterotoxin and the lecithinase of Clostridium perfringens and their application to the determination of the presence and numeration of these bacteriae
US5496470A (en) * 1994-05-27 1996-03-05 Barnes International, Inc. Magnetic separator
US6037465A (en) * 1994-06-14 2000-03-14 Invitek Gmbh Universal process for isolating and purifying nucleic acids from extremely small amounts of highly contaminated various starting materials
US5512441A (en) * 1994-11-15 1996-04-30 American Health Foundation Quantative method for early detection of mutant alleles and diagnostic kits for carrying out the method
US5599662A (en) * 1995-02-17 1997-02-04 Hoffmann-La Roche Inc. Oliconucleotide primers and probes for the detection of HIV-1
US6084091A (en) * 1995-08-16 2000-07-04 Max-Planck-Gesellschaft Zur Forerung Der Wissenschaften E.V. Process for purifying, stabilising or isolating nucleic acids from biological materials
US5612473A (en) * 1996-01-16 1997-03-18 Gull Laboratories Methods, kits and solutions for preparing sample material for nucleic acid amplification
US5741650A (en) * 1996-01-30 1998-04-21 Exact Laboratories, Inc. Methods for detecting colon cancer from stool samples
US5882865A (en) * 1996-03-22 1999-03-16 The Johns Hopkins University Cancer drug screen based on cell cycle uncoupling
US5645995A (en) * 1996-04-12 1997-07-08 Baylor College Of Medicine Methods for diagnosing an increased risk for breast or ovarian cancer
US6203993B1 (en) * 1996-08-14 2001-03-20 Exact Science Corp. Methods for the detection of nucleic acids
US20020119469A1 (en) * 1996-08-14 2002-08-29 Shuber Anthony P. Methods for the detection of nucleic acids
US5952178A (en) * 1996-08-14 1999-09-14 Exact Laboratories Methods for disease diagnosis from stool samples
US6020137A (en) * 1996-08-14 2000-02-01 Exact Laboratories, Inc. Methods for the detection of loss of heterozygosity
US6214558B1 (en) * 1996-08-14 2001-04-10 Exact Laboratories, Inc. Methods for the detection of chromosomal aberrations
US5670325A (en) * 1996-08-14 1997-09-23 Exact Laboratories, Inc. Method for the detection of clonal populations of transformed cells in a genomically heterogeneous cellular sample
US6100029A (en) * 1996-08-14 2000-08-08 Exact Laboratories, Inc. Methods for the detection of chromosomal aberrations
US6448002B1 (en) * 1996-08-26 2002-09-10 Invitek Gmbh Method to detect clinically relevant mutations of the DNA sequence of ki-ras oncogene, its use and a testkit for early diagnosis of tumors
US5856104A (en) * 1996-10-28 1999-01-05 Affymetrix, Inc. Polymorphisms in the glucose-6 phosphate dehydrogenase locus
US6235474B1 (en) * 1996-12-30 2001-05-22 The Johns Hopkins University Methods and kits for diagnosing and determination of the predisposition for diseases
US6268136B1 (en) * 1997-06-16 2001-07-31 Exact Science Corporation Methods for stool sample preparation
US6406857B1 (en) * 1997-06-16 2002-06-18 Exact Sciences Corporation Methods for stool sample preparation
US5888778A (en) * 1997-06-16 1999-03-30 Exact Laboratories, Inc. High-throughput screening method for identification of genetic mutations or disease-causing microorganisms using segmented primers
US5928870A (en) * 1997-06-16 1999-07-27 Exact Laboratories, Inc. Methods for the detection of loss of heterozygosity
US20020004201A1 (en) * 1997-06-16 2002-01-10 Lapidus Stanley N. Methods for the detection of loss of heterozygosity
US5942396A (en) * 1997-08-19 1999-08-24 The Rockefeller University Method for identifying individuals at risk for colorectal neoplasia by quantifying normal colonic mucosal epithelial cell apoptosis
US20030087258A1 (en) * 1997-10-23 2003-05-08 Shuber Anthony P. Methods for detecting hypermethylated nucleic acid in heterogeneous biological samples
US20020025525A1 (en) * 1997-10-23 2002-02-28 Shuber Anthony P. Methods for detecting contamination in molecular diagnostics using PCR
US6251660B1 (en) * 1997-11-25 2001-06-26 Mosaic Technologies, Inc. Devices and methods for detecting target molecules in biological samples
US6228596B1 (en) * 1998-03-05 2001-05-08 Diadexus, Inc. Method of detecting and monitoring endometrial and uterine cancers
US6214187B1 (en) * 1998-06-18 2001-04-10 Mosaic Technologies Denaturing gradient affinity electrophoresis and methods of use thereof
US20020001800A1 (en) * 1998-08-14 2002-01-03 Stanley N. Lapidus Diagnostic methods using serial testing of polymorphic loci
US6238927B1 (en) * 1998-10-05 2001-05-29 Mosaic Technologies, Incorporated Reverse displacement assay for detection of nucleic acid sequences
US20030044780A1 (en) * 1998-11-23 2003-03-06 Stanley N. Lapidus Primer extension methods utilizing donor and acceptor molecules for detecting nucleic acids
US20020048752A1 (en) * 1998-11-23 2002-04-25 Stanley N. Lapidus Methods for detecting lower-frequency molecules
US20020123052A1 (en) * 1999-01-10 2002-09-05 Steven Laken Methods for detecting mutations using primer extension for detecting disease
US6503718B2 (en) * 1999-01-10 2003-01-07 Exact Sciences Corporation Methods for detecting mutations using primer extension for detecting disease
US20010018180A1 (en) * 1999-01-10 2001-08-30 Shuber Anthony P. Methods for detecting mutations using primer extension for detecting disease
US20020064787A1 (en) * 1999-01-10 2002-05-30 Shuber Anthony P. Methods for detecting mutations using primer extension for detecting disease
US6551777B1 (en) * 1999-02-25 2003-04-22 Exact Sciences Corporation Methods for preserving DNA integrity
US6415455B1 (en) * 1999-05-03 2002-07-09 Exact Sciences Corporation Stool specimen collector
US6351857B2 (en) * 1999-05-03 2002-03-05 Exact Sciences Corporation Stool specimen collector
US20020045183A1 (en) * 1999-08-11 2002-04-18 Shuber Anthony P. Methods for detecting mutations using primer extension
US6280947B1 (en) * 1999-08-11 2001-08-28 Exact Sciences Corporation Methods for detecting nucleotide insertion or deletion using primer extension
US6586177B1 (en) * 1999-09-08 2003-07-01 Exact Sciences Corporation Methods for disease detection
US6849403B1 (en) * 1999-09-08 2005-02-01 Exact Sciences Corporation Apparatus and method for drug screening
US20070202513A1 (en) * 1999-09-08 2007-08-30 Exact Sciences Corporation Methods for disease detection
US20040043467A1 (en) * 1999-12-07 2004-03-04 Shuber Anthony P. Supracolonic aerodigestive neoplasm detection
US6919174B1 (en) * 1999-12-07 2005-07-19 Exact Sciences Corporation Methods for disease detection
US20060121495A1 (en) * 1999-12-07 2006-06-08 Exact Sciences Corporation Methods for disease detection
US20020019472A1 (en) * 2000-06-13 2002-02-14 Fumio Yamashita Copolymer excelling in pigment dispersibility
US20020110810A1 (en) * 2001-01-05 2002-08-15 Shuber Anthony P. Methods for detecting, grading or monitoring an H. pylori infection
US20020132251A1 (en) * 2001-03-15 2002-09-19 Shuber Anthony P. Method for alteration detection
US6428964B1 (en) * 2001-03-15 2002-08-06 Exact Sciences Corporation Method for alteration detection
US20030049659A1 (en) * 2001-05-29 2003-03-13 Lapidus Stanley N. Devices and methods for isolating samples into subsamples for analysis

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080206756A1 (en) * 2003-07-18 2008-08-28 California Pacific Medical Center Biomarker panel for colorectal cancer
US20050014165A1 (en) * 2003-07-18 2005-01-20 California Pacific Medical Center Biomarker panel for colorectal cancer
USRE49542E1 (en) * 2005-04-06 2023-06-06 Guardant Health, Inc. Method for the detection of cancer
US20100124743A1 (en) * 2007-01-23 2010-05-20 Olympus Corporation Method for diagnosis of cancer
US10400283B2 (en) 2007-05-31 2019-09-03 Nancy M. Lee Method to predict or diagnose a gastrointestinal disorder or disease
US10011879B2 (en) 2007-07-26 2018-07-03 Nancy M. Lee Method to predict or diagnose a gastointestinal disorder or disease
US20100261221A1 (en) * 2007-07-26 2010-10-14 California Pacific Medical Center Method to predict or diagnose a gastrointestinal disorder or disease
US8883440B2 (en) 2007-07-26 2014-11-11 Nancy M. Lee Method to predict or diagnose a gastrointestinal disorder or disease
US9353420B2 (en) 2007-07-26 2016-05-31 Nancy M. Lee Method to predict or diagnose a gastointestinal disorder or disease
US20100255481A1 (en) * 2007-10-30 2010-10-07 Olympus Corporation Method for detection of adenoma or cancer by genetic analysis
WO2009104714A1 (en) * 2008-02-22 2009-08-27 株式会社ジーンサイエンス Early genetic test method for cancer
KR20160019419A (en) 2013-05-08 2016-02-19 유겐가이샤 마이테크 Raman quantification method of cancer-related substance
US9535069B2 (en) 2013-05-08 2017-01-03 Mytech Co., Ltd. Method of measuring cancer related substances by raman spectroscopy
KR102162706B1 (en) 2013-05-08 2020-10-07 유겐가이샤 마이테크 Raman quantification method of cancer-related substance
WO2014181816A1 (en) 2013-05-08 2014-11-13 有限会社マイテック Raman quantification method of cancer-related substance
CN107208159A (en) * 2015-01-30 2017-09-26 恩特姆生物科学公司 Host DNA as Crohn's disease biomarker
US9873914B2 (en) 2015-01-30 2018-01-23 Enterome Host DNA as a biomarker of Crohn's disease
WO2016120475A1 (en) * 2015-01-30 2016-08-04 Enterome Host dna as a biomarker of crohn's disease
US10793911B2 (en) 2015-01-30 2020-10-06 Enterome Host DNA as a biomarker of Crohn's disease

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